Clinical studies index
Every study cited across the library, in one searchable table, 905 records covering 196 compounds. Each links out to PubMed, the DOI or the trial registry.
Why we link rather than host
Published papers are copyrighted by their journals. We record the citation, the design, the sample size and the finding, and send you to the source, which is also where you can check whether we have characterised it fairly. Where a paper is open access, the DOI link will reach the full text directly.
| Compound | Study | Year | Design | Tier | Source |
|---|---|---|---|---|---|
| Abaloparatide | Effect of abaloparatide vs placebo on new vertebral fractures in postmenopausal women with osteoporosis: a randomized clinical trial | 2016 | Randomised, double-blind, placebo-controlled phase 3 trial with open-label teriparatide comparator; n=2,463 postmenopausal women; 18 months. Published as 316(7):722-33. | PMID DOI Trial | |
| Abaloparatide | Eighteen months of treatment with subcutaneous abaloparatide followed by 6 months of treatment with alendronate in postmenopausal women with osteoporosis: results of the ACTIVExtend trial | 2017 | Pre-specified open-label extension of ACTIVE; 18 months of abaloparatide followed by 6 months of alendronate versus placebo followed by alendronate (approximately 25 months total). Published as 92(2):200-210. | PMID DOI Trial | |
| Abaloparatide | Fracture and bone mineral density response by baseline risk in patients treated with abaloparatide followed by alendronate: results from the phase 3 ACTIVExtend trial | 2019 | Pre-specified subgroup analysis of the ACTIVExtend extension by baseline fracture risk. Published as 34(12):2213-2219. | PMID DOI | |
| Abaloparatide | The efficacy and safety of abaloparatide-SC in men with osteoporosis: a randomized clinical trial | 2022 | Randomised, double-blind, placebo-controlled phase 3 trial in men with osteoporosis (ATOM); 12 months. Published as 37(12):2435-2442. | PMID DOI | |
| Abaloparatide | Abaloparatide increases lumbar spine and hip BMD in Japanese patients with osteoporosis: the phase 3 ACTIVE-J study | 2022 | Randomised, double-blind, placebo-controlled phase 3 trial in a Japanese osteoporosis population; 18 months. Published as 107(10):e4222-e4231. | PMID DOI | |
| ACE-031 (soluble ActRIIB-IgG1 Fc fusion protein) | A single ascending-dose study of muscle regulator ACE-031 in healthy volunteers | 2013 | Randomised, double-blind, placebo-controlled single ascending dose; n=48 healthy postmenopausal women receiving ACE-031 0.02-3 mg/kg subcutaneously or placebo | Mixed evidence | PMID DOI Trial |
| ACE-031 (soluble ActRIIB-IgG1 Fc fusion protein) | Myostatin inhibitor ACE-031 treatment of ambulatory boys with Duchenne muscular dystrophy: Results of a randomized, placebo-controlled clinical trial | 2017 | Randomised, double-blind, placebo-controlled ascending-dose trial with open-label extension in ambulatory boys with Duchenne muscular dystrophy; ACE-031 given subcutaneously; terminated after the second dosing regimen | Mixed evidence | PMID DOI Trial |
| ACE-031 (soluble ActRIIB-IgG1 Fc fusion protein) | Regulation of muscle growth by multiple ligands signaling through activin type II receptors | 2005 | Soluble ActRIIB administration in wild-type and myostatin-null mice | Preclinical only | PMID DOI |
| ACE-031 (soluble ActRIIB-IgG1 Fc fusion protein) | Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy | 2014 | ActRIIB blockade in mice with functional and metabolic phenotyping of hypertrophied muscle | Preclinical only | PMID DOI |
| ACE-031 (soluble ActRIIB-IgG1 Fc fusion protein) | Treatment with soluble activin type IIB-receptor improves bone mass and strength in a mouse model of Duchenne muscular dystrophy | 2017 | Soluble ActRIIB administration in the mdx mouse model with bone densitometry and mechanical testing | Preclinical only | PMID DOI |
| ACE-031 (soluble ActRIIB-IgG1 Fc fusion protein) | Combined detection of inhibitors of the activin receptor signaling pathways (IASPs) by means of LC-HRMS/MS for human doping control | 2025 | Analytical method development and validation for doping-control detection of activin receptor pathway inhibitors | Limited evidence | PMID DOI |
| Acetyl hexapeptide-8 | A synthetic hexapeptide (Argireline) with antiwrinkle activity | 2002 | Mechanistic cell-based work plus in vivo skin topography analysis in healthy women volunteers; 10% hexapeptide in an oil-in-water emulsion, 30 days | Mixed evidence | PMID DOI |
| Acetyl hexapeptide-8 | The anti-wrinkle efficacy of argireline, a synthetic hexapeptide, in Chinese subjects: a randomized, placebo-controlled study | 2013 | Randomised, placebo-controlled; n=60 Chinese subjects allocated 3:1 to peptide or placebo; twice-daily periorbital application for 4 weeks; subjective global assessment plus objective silicone-replica wrinkle analysis | Mixed evidence | PMID DOI |
| Acetyl hexapeptide-8 | In vitro skin penetration of acetyl hexapeptide-8 from a cosmetic formulation | 2015 | In vitro diffusion cells using excised human cadaver and hairless guinea pig skin; 10% Ac-EEMQRR-amide oil-in-water emulsion at 2 mg/cm2; 24-hour exposure; tape stripping and LC-MS/MS quantification | Preclinical only | PMID DOI |
| Acetyl hexapeptide-8 | Topical delivery of acetyl hexapeptide-8 from different emulsions: influence of emulsion composition and internal structure | 2015 | Franz-type diffusion cell permeation experiments plus in vitro tape stripping on porcine ear skin, comparing oil-in-water, water-in-oil and multiple water-in-oil-in-water emulsions; LC-MS/MS quantification | Preclinical only | PMID DOI |
| Acetyl hexapeptide-8 | Acetyl Hexapeptide-8 in Cosmeceuticals-A Review of Skin Permeability and Efficacy | 2025 | Narrative review of the structure, permeability and efficacy literature | Mixed evidence | PMID DOI |
| Acetyl hexapeptide-8 | The efficacy study of the combination of tripeptide-10-citrulline and acetyl hexapeptide-3. A prospective, randomized controlled study | 2017 | Prospective randomised controlled study, four arms of six volunteers (n=24), 60 days; skin microtopography (cR2, cR3) by visioscan and transepidermal water loss by tewameter | Limited evidence | PMID DOI |
| Acetyl hexapeptide-8 | Skin scars and wrinkles temporary camouflage in dermatology and oncoesthetics: focus on acetyl hexapeptide-8 | 2020 | Described by its authors as a spontaneous, anecdotal, retrospective study of 26 patients using a 10% acetyl hexapeptide-8 gel-cream on surgical scars and skin lesions; no control group | Limited evidence | PMID DOI |
| Acetyl hexapeptide-8 | Double-blind, Randomized Trial on the Effectiveness of Acetylhexapeptide-3 Cream and Palmitoyl Pentapeptide-4 Cream for Crow's Feet | 2023 | Double-blind randomised trial, three arms of 7 subjects (n=21), 8 weeks, twice-daily periorbital application | Limited evidence | PMID |
| Acetyl octapeptide-3 | A synthetic hexapeptide (Argireline) with antiwrinkle activity | 2002 | Mechanistic cell-based work plus in vivo skin topography in healthy women volunteers; 10% hexapeptide oil-in-water emulsion, 30 days | Mixed evidence | PMID DOI |
| Acetyl octapeptide-3 | Efficacy of bioactive peptides loaded on hyaluronic acid microneedle patches: A monocentric clinical study | 2020 | Monocentric 12-week study, no placebo or comparator arm, of a multi-ingredient hyaluronic acid microneedle patch containing acetyl octapeptide-3 alongside arginine/lysine polypeptide, palmitoyl tripeptide-5, adenosine and seaweed extracts; instrumental skin measurements | Limited evidence | PMID DOI |
| Acetyl octapeptide-3 | In vitro skin penetration of acetyl hexapeptide-8 from a cosmetic formulation | 2015 | In vitro diffusion cells, excised human cadaver and hairless guinea pig skin, 24-hour exposure to a 10% oil-in-water emulsion at 2 mg/cm2 | Preclinical only | PMID DOI |
| Acetyl octapeptide-3 | Acetyl Hexapeptide-8 in Cosmeceuticals-A Review of Skin Permeability and Efficacy | 2025 | Narrative review of permeability and efficacy data for the SNAP-25-mimetic cosmetic peptide class | Mixed evidence | PMID DOI |
| acetyl tetrapeptide-5 | Protective and Anti-Aging Effects of 5 Cosmeceutical Peptide Mixtures on Hydrogen Peroxide-Induced Premature Senescence in Human Skin Fibroblasts | 2021 | In vitro, human skin fibroblasts; five peptides tested individually for optimal concentration, then six mixtures tested | Preclinical only | PMID DOI |
| acetyl tetrapeptide-5 | Physiology and pathophysiology of carnosine | 2013 | Comprehensive review | PMID | |
| acetyl tetrapeptide-5 | Glycation, ageing and carnosine: are carnivorous diets beneficial? | 2005 | Review and hypothesis | PMID | |
| acetyl tetrapeptide-5 | Carnosine and carnosine-related antioxidants: a review | 2005 | Chemistry review | PMID | |
| Adipotide | Reversal of obesity by targeted ablation of adipose tissue | 2004 | Preclinical; phage display target identification and treatment of obese mouse models | Preclinical only | PMID DOI |
| Adipotide | A peptidomimetic targeting white fat causes weight loss and improved insulin resistance in obese monkeys | 2011 | Preclinical; spontaneously obese rhesus monkeys, four weeks of treatment | Preclinical only | PMID DOI |
| Adipotide | Comment on 'A peptidomimetic targeting white fat causes weight loss and improved insulin resistance in obese monkeys' | 2012 | Published methodological commentary, with author reply | Preclinical only | PMID DOI |
| Adipotide | A First-in-Man, Phase I Evaluation of A Single Cycle of Prohibitin Targeting Peptide 1 in Patients With Metastatic Prostate Cancer and Obesity | 2011 | Phase 1, single-cycle, first-in-human study, n=4, terminated | Limited evidence | Trial |
| Adipotide | Depletion of white adipocyte progenitors induces beige adipocyte differentiation and suppresses obesity development | 2015 | Preclinical; mouse models of targeted adipose progenitor depletion | Preclinical only | PMID DOI |
| Adrenomedullin | Adrenomedullin: a novel hypotensive peptide isolated from human pheochromocytoma | 1993 | Peptide isolation and structural characterisation using platelet cyclic AMP bioassay | PMID | |
| Adrenomedullin | Safety and tolerability of non-neutralizing adrenomedullin antibody adrecizumab (HAM8101) in septic shock patients: the AdrenOSS-2 phase 2a biomarker-guided trial | 2021 | Phase 2a randomised double-blind placebo-controlled biomarker-guided trial, 301 patients with septic shock, randomisation 1:1:2 | PMID DOI | |
| Adrenomedullin | Effects of enrichment strategies on outcome of adrecizumab treatment in septic shock: Post-hoc analyses of the phase II AdrenOSS-2 trial | 2022 | Post-hoc biomarker-guided subgroup analysis of a phase 2 trial | PMID DOI | |
| Afamelanotide | Afamelanotide for Erythropoietic Protoporphyria | 2015 | Two multicentre randomised, double-blind, placebo-controlled trials of 16 mg subcutaneous implants every 60 days; n=74 (EU, 270 days) and n=94 (US, 180 days) | High-quality evidence | PMID DOI |
| Afamelanotide | Long-term observational study of afamelanotide in 115 patients with erythropoietic protoporphyria | 2015 | Multicentre longitudinal observational study at two porphyria centres (Rome and Zurich); 115 patients, 1,023 implants, up to 8 years | Mixed evidence | PMID DOI |
| Afamelanotide | Afamelanotide and narrowband UV-B phototherapy for the treatment of vitiligo: a randomized multicenter trial | 2015 | Randomised multicentre trial, n=55 (28 combination, 27 monotherapy), afamelanotide implant plus narrowband UVB versus narrowband UVB alone | Mixed evidence | PMID DOI |
| Afamelanotide | Discovery and development of novel melanogenic drugs. Melanotan-I and -II | 1998 | Review of the preclinical design and development of the melanotan analogues | Preclinical only | PMID DOI |
| Alarelin | Comparison of Alarelin and Triptorelin in the long-protocol ovulation induction in in vitro fertilization and embryo transfer | 2010 | Comparative clinical study in 122 infertile patients undergoing IVF-ET: 78 received alarelin, 44 received triptorelin, long downregulation protocol | PMID | |
| Alarelin | Pharmacogenomic analysis of alarelin acetate-induced hepatotoxicity: a case report and literature review | 2025 | Single clinical case report with RUCAM causality assessment, pharmacogenomic analysis and literature review | PMID DOI | |
| Alarelin | Liquid chromatography tandem mass spectrometry with triple stage fragmentation for highly selective analysis and pharmacokinetics of alarelin in rat plasma | 2019 | Bioanalytical method development with a rat pharmacokinetic study after a 13.5 microgram/kg intramuscular dose | Preclinical only | PMID DOI |
| Alarelin | Alarelin active immunization influences expression levels of GnRHR, FSHR and LHR proteins in the ovary and enhances follicular development in ewes | 2013 | Controlled active immunisation study in pre-pubertal ewes at varying doses and frequencies against a control group | Preclinical only | PMID DOI |
| Alarelin | Induction of Spermiation in Sterlet Acipenser ruthenus by PLGA Microparticle Delivery with Sustained Alarelin Release | 2021 | Controlled experimental study in sterlet comparing carp pituitary extract with two doses of alarelin in PLGA sustained-release microparticles | Preclinical only | PMID DOI |
| Albiglutide | Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial | 2018 | Randomised, double-blind, placebo-controlled cardiovascular outcomes trial, 9,463 participants with established cardiovascular disease, median follow-up 1.6 years | PMID DOI Trial | |
| Albiglutide | Once-weekly albiglutide versus once-daily liraglutide in patients with type 2 diabetes inadequately controlled on oral drugs (HARMONY 7): a randomised, open-label, multicentre, non-inferiority phase 3 study | 2014 | 32-week randomised, open-label, active-comparator non-inferiority phase 3 trial across 162 sites in eight countries, 841 adults (albiglutide 422, liraglutide 419) | PMID DOI | |
| Albiglutide | HARMONY 3: 104-week randomized, double-blind, placebo- and active-controlled trial assessing the efficacy and safety of albiglutide compared with placebo, sitagliptin, and glimepiride in patients with type 2 diabetes taking metformin | 2014 | 104-week randomised, double-blind, placebo- and active-controlled phase 3 trial, approximately 1,012 adults (albiglutide 302, glimepiride 307, sitagliptin 302, placebo 101) | PMID DOI | |
| Albiglutide | HARMONY 4: randomised clinical trial comparing once-weekly albiglutide and insulin glargine in patients with type 2 diabetes inadequately controlled with metformin with or without sulfonylurea | 2014 | 52-week randomised, open-label, multicentre, parallel-group non-inferiority trial across 222 centres in four countries, 779 adults randomised 2:1 (albiglutide 504, insulin glargine 241) | PMID DOI | |
| Albiglutide | Efficacy and safety of once-weekly GLP-1 receptor agonist albiglutide (HARMONY 2): 52 week primary endpoint results from a randomised, placebo-controlled trial in patients with type 2 diabetes mellitus inadequately controlled with diet and exercise | 2016 | 52-week randomised, double-blind, placebo-controlled monotherapy trial, 309 adults (albiglutide 30 mg n=102, albiglutide 50 mg n=102, placebo n=105) | PMID DOI | |
| Anamorelin | Anamorelin in patients with non-small-cell lung cancer and cachexia (ROMANA 1 and ROMANA 2): results from two randomised, double-blind, phase 3 trials | 2016 | Two randomised, double-blind, placebo-controlled phase 3 trials at 93 sites in 19 countries; 484 patients in ROMANA 1 (323 anamorelin, 161 placebo) and 495 in ROMANA 2 (330 anamorelin, 165 placebo), randomised 2:1 to anamorelin 100 mg orally once daily or placebo for 12 weeks, with co-primary endpoints of median change in lean body mass and in handgrip strength | PMID DOI Trial | |
| Anamorelin | ROMANA 3: a phase 3 safety extension study of anamorelin in advanced non-small-cell lung cancer (NSCLC) patients with cachexia | 2017 | Twelve-week double-blind safety extension for patients with preserved performance status completing ROMANA 1 or ROMANA 2, extending exposure from 12 to 24 weeks; of 703 patients completing the core trials, 513 entered (anamorelin 345, placebo 168) | PMID DOI | |
| Anamorelin | The regulatory approval of anamorelin for treatment of cachexia in patients with non-small cell lung cancer, gastric cancer, pancreatic cancer, and colorectal cancer in Japan: facts and numbers | 2021 | Regulatory analysis of the Japanese approval decision and the supporting Japanese trial programme | PMID DOI | |
| Anamorelin | Anamorelin in Japanese patients with cancer cachexia: an update | 2023 | Narrative review of post-approval Japanese clinical experience with anamorelin | PMID DOI | |
| Angiotensin II | Angiotensin II for the treatment of vasodilatory shock | 2017 | Multicentre, randomised, double-blind, placebo-controlled phase 3 trial; 321 patients with vasodilatory shock requiring high-dose vasopressors | PMID DOI | |
| Angiotensin II | Intravenous angiotensin II for the treatment of high-output shock (ATHOS trial): a pilot study | 2014 | Randomised, double-blind, placebo-controlled pilot; 20 patients with high-output shock (10 angiotensin II, 10 placebo) | PMID DOI | |
| AOD-9604 | Hyperglycemic action of synthetic C-terminal fragments of human growth hormone | 1978 | Preclinical; synthetic peptide fragments in animal models | Preclinical only | PMID DOI |
| AOD-9604 | Effects of oral administration of a synthetic fragment of human growth hormone on lipid metabolism | 2000 | Preclinical; oral administration in rodent models | Preclinical only | PMID DOI |
| AOD-9604 | The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta(3)-AR knock-out mice | 2001 | Preclinical; chronic dosing in obese mice and beta-3 adrenergic receptor knockout mice | Preclinical only | PMID DOI |
| AOD-9604 | Metabolic studies of a synthetic lipolytic domain (AOD9604) of human growth hormone | 2000 | Preclinical metabolic characterisation | Preclinical only | PMID DOI |
| AOD-9604 | Safety and Tolerability of the Hexadecapeptide AOD9604 in Humans | 2013 | Pooled review of six randomised, double-blind, placebo-controlled human trials | Limited evidence | DOI |
| AOD-9604 | Phase 2b obesity trial of AOD9604 (unpublished; sponsor-reported) | 2007 | Randomised, double-blind, placebo-controlled obesity trial using oral administration over 24 weeks in several hundred participants; sponsor disclosures indicate an enrolment in the region of 500, which this audit could not independently confirm | Limited evidence | none |
| AOD-9604 | Effect of Intra-articular Injection of AOD9604 with or without Hyaluronic Acid in Rabbit Osteoarthritis Model | 2015 | Preclinical; rabbit osteoarthritis model | Preclinical only | PMID |
| Apelin-13 | Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor | 1998 | Peptide isolation from bovine stomach extracts with receptor deorphanisation | PMID | |
| Apelin-13 | Acute cardiovascular effects of apelin in humans: potential role in patients with chronic heart failure | 2010 | Randomised placebo-controlled systemic and intracoronary infusion studies in heart failure patients and healthy controls | PMID | |
| Apelin-13 | In Vitro and In Vivo Evaluation of a Small-Molecule APJ (Apelin Receptor) Agonist, BMS-986224, as a Potential Treatment for Heart Failure | 2021 | In vitro pharmacology and animal haemodynamic studies | Preclinical only | PMID |
| Apelin-13 | A study of CLR325 in chronic stable heart failure patients | 2016 | Phase 2 randomised placebo-controlled study of a cyclic apelin-13 analogue; registration status listed as completed | Trial | |
| B7-33 | A single-chain derivative of the relaxin hormone is a functionally selective agonist of the G protein-coupled receptor, RXFP1 | 2016 | Peptide design and synthesis, receptor binding and signalling assays, three preclinical rodent models of heart and lung disease | Preclinical only | PMID DOI |
| B7-33 | B7-33 replicates the vasoprotective functions of human relaxin-2 (serelaxin) | 2017 | Rat tail-vein bolus with wire myography of mesenteric, small renal and abdominal aortic vessels; ex vivo mouse preeclampsia model | Preclinical only | PMID DOI |
| B7-33 | The single-chain relaxin mimetic, B7-33, maintains the cardioprotective effects of relaxin and more rapidly reduces left ventricular fibrosis compared to perindopril in an experimental model of cardiomyopathy | 2023 | Isoprenaline-induced cardiomyopathy in adult male 129sv mice; subcutaneous relaxin, B7-33 or perindopril from days 7-14 post-injury | Preclinical only | PMID DOI |
| B7-33 | A Lipidated Single-B-Chain Derivative of Relaxin Exhibits Improved In Vitro Serum Stability without Altering Activity | 2023 | Peptide chemistry and in vitro serum stability assays | Preclinical only | PMID DOI |
| B7-33 | Effects of Serelaxin in Patients with Acute Heart Failure | 2019 | RELAX-AHF-2: large randomised double-blind placebo-controlled Phase 3 trial of recombinant human relaxin-2 | High-quality evidence | PMID DOI |
| Bacitracin | Infection and allergy incidence in ambulatory surgery patients using white petrolatum vs bacitracin ointment. A randomized controlled trial | 1996 | Randomised, double-blind controlled trial in ambulatory dermatological surgery patients; 922 patients with 1249 wounds (440 evaluable petrolatum, 444 evaluable bacitracin), JAMA 276(12):972-7 | PMID | |
| Bacitracin | FDA Antimicrobial Drugs Advisory Committee review of bacitracin for injection | 2019 | Regulatory advisory committee review of accumulated safety and efficacy data | none | |
| Bacitracin | FDA request for voluntary withdrawal of all bacitracin for injection applications | 2020 | Regulatory action | none | |
| Bacitracin | Determination that bacitracin for injection was withdrawn from sale for reasons of safety or effectiveness | 2022 | Formal regulatory determination | none | |
| Beta-endorphin | Isolation and structure of an untriakontapeptide with opiate activity from camel pituitary glands | 1976 | Peptide isolation and structural determination | PMID | |
| Beta-endorphin | The runner's high: opioidergic mechanisms in the human brain | 2008 | PET ligand activation study in ten athletes, scanned at rest and after two hours of endurance running | PMID | |
| Beta-endorphin | Neuropharmacological dissection of placebo analgesia: expectation-activated opioid systems versus conditioning-activated specific subsystems | 1999 | Human experimental pain study with naloxone blockade | PMID DOI | |
| Bivalirudin | Bivalirudin for patients with acute coronary syndromes | 2006 | Prospective, open-label, randomised trial; 13,819 patients with moderate- to high-risk acute coronary syndromes randomised to heparin plus GPIIb/IIIa inhibitor, bivalirudin plus GPIIb/IIIa inhibitor, or bivalirudin alone | PMID DOI Trial | |
| Bivalirudin | Bivalirudin during primary PCI in acute myocardial infarction | 2008 | Open-label randomised trial; 3,602 patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention | PMID DOI | |
| Bivalirudin | Unfractionated heparin versus bivalirudin in primary percutaneous coronary intervention (HEAT-PPCI): an open-label, single centre, randomised controlled trial | 2014 | Open-label, single-centre randomised controlled trial; 1,829 patients randomly allocated (1,812 analysed: 905 bivalirudin, 907 heparin) undergoing primary PCI | PMID DOI | |
| Bivalirudin | Bivalirudin or unfractionated heparin in acute coronary syndromes | 2015 | Multicentre randomised trial; 7,213 patients with acute coronary syndromes undergoing PCI, with a second randomisation to post-PCI bivalirudin infusion or no infusion | PMID DOI | |
| Bivalirudin | Bivalirudin versus heparin monotherapy in myocardial infarction | 2017 | Multicentre, registry-based, open-label randomised clinical trial; 6,006 patients (3,005 STEMI, 3,001 NSTEMI) undergoing PCI with predominantly radial access and no routine GPIIb/IIIa inhibitor | PMID DOI | |
| Bivalirudin | Bivalirudin plus a high-dose infusion versus heparin monotherapy in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention: a randomised trial | 2022 | Multicentre, open-label, randomised trial; 6,016 patients with STEMI undergoing primary PCI in China (3,009 bivalirudin plus post-PCI infusion, 3,007 heparin monotherapy) | PMID DOI | |
| bortezomib | A phase 2 study of bortezomib in relapsed, refractory myeloma | 2003 | Open-label single-arm phase 2 (SUMMIT), 202 patients with heavily pre-treated relapsed/refractory multiple myeloma (193 evaluable) | PMID | |
| bortezomib | Bortezomib or high-dose dexamethasone for relapsed multiple myeloma | 2005 | Randomised open-label phase 3 (APEX), 669 patients with one to three prior therapies | PMID DOI | |
| bortezomib | Bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma | 2008 | Randomised open-label phase 3 (VISTA), 682 previously untreated patients ineligible for transplantation | PMID DOI | |
| bortezomib | Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: a randomised, phase 3, non-inferiority study | 2011 | Randomised phase 3 non-inferiority trial, 222 patients randomised 2:1 to subcutaneous or intravenous bortezomib | PMID DOI | |
| BPC-157 | Emerging Use of BPC-157 in Orthopaedic Sports Medicine: A Systematic Review | 2025 | Systematic review of literature to 3 June 2024; 544 articles identified, 36 included (35 preclinical, 1 clinical) | Limited evidence | PMID DOI |
| BPC-157 | The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration | 2011 | In vitro rat Achilles tendon fibroblast culture plus in vivo rat tendon transection | Preclinical only | PMID DOI |
| BPC-157 | Pentadecapeptide BPC 157 enhances the growth hormone receptor expression in tendon fibroblasts | 2014 | In vitro rat tendon fibroblast culture, dose- and time-response | Preclinical only | PMID DOI |
| BPC-157 | Stable Gastric Pentadecapeptide BPC 157 and Wound Healing | 2021 | Narrative review from the originating research group | Preclinical only | PMID DOI |
| BPC-157 | Stable gastric pentadecapeptide BPC 157 in trials for inflammatory bowel disease (PL-10, PLD-116, PL 14736, Pliva, Croatia). Full and distended stomach, and vascular response | 2006 | Review with rat gastric distension and vascular experiments | Preclinical only | PMID DOI |
| BPC-157 | Safety of Intravenous Infusion of BPC157 in Humans: A Pilot Study | 2025 | Uncontrolled open-label pilot, n=2 healthy adults, 10 mg then 20 mg intravenous infusions | Limited evidence | PMID |
| Bradykinin | Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema | 2010 | Two randomised double-blind controlled trials (FAST-1 and FAST-2) | PMID | |
| Bradykinin | Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks | 2024 | Randomised double-blind placebo-controlled three-way crossover phase 3 trial (KONFIDENT) | PMID DOI Trial | |
| Bradykinin | Randomized Trial of Icatibant for Angiotensin-Converting Enzyme Inhibitor-Induced Upper Airway Angioedema | 2017 | Multicentre randomised double-blind placebo-controlled trial at 31 centres in 4 countries, 121 patients (icatibant n=61, placebo n=60) | PMID DOI | |
| Bremelanotide | Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials | 2019 | Two identical randomised, double-blind, placebo-controlled 24-week phase 3 trials (RECONNECT); 1,267 premenopausal women randomised, 1,202 in the modified intent-to-treat efficacy population | High-quality evidence | PMID DOI |
| Bremelanotide | Long-Term Safety and Efficacy of Bremelanotide for Hypoactive Sexual Desire Disorder | 2019 | 52-week open-label extension of the RECONNECT phase 3 trials; 684 of 856 eligible women enrolled, 272 completed | Mixed evidence | PMID DOI |
| Bremelanotide | Responder Analyses from a Phase 2b Dose-Ranging Study of Bremelanotide | 2019 | Post hoc responder analysis of a randomised, double-blind, placebo-controlled phase 2b dose-ranging trial in premenopausal women with hypoactive sexual desire disorder and/or female sexual arousal disorder | Mixed evidence | PMID DOI |
| Bremelanotide | Salvage of sildenafil failures with bremelanotide: a randomized, double-blind, placebo controlled study | 2008 | Randomised, double-blind, placebo-controlled trial of intranasal bremelanotide in 342 men aged 28-59 with erectile dysfunction unresponsive to sildenafil (172 bremelanotide, 170 placebo) | Limited evidence | PMID DOI |
| Bronchogen | Modulating Effect of Peptide Therapy on the Morphofunctional State of Bronchial Epithelium in Rats with Obstructive Lung Pathology | 2015 | Rat model of chronic obstructive pulmonary disease induced by 60 days of intermittent nitrogen dioxide exposure, followed by one month of Bronchogen | Preclinical only | PMID DOI |
| Bronchogen | Effect of the peptide bronchogen (Ala-Asp-Glu-Leu) on DNA thermostability | 2011 | Biophysical, differential scanning calorimetry of DNA | Preclinical only | PMID DOI |
| Bronchogen | Penetration of short fluorescence-labeled peptides into the nucleus in HeLa cells and in vitro specific interaction of the peptides with deoxyribooligonucleotides and DNA | 2011 | In vitro, fluorescence quenching against labelled deoxyribo-oligonucleotides and DNA | Preclinical only | PMID DOI |
| Bronchogen | Short Exogenous Peptides Regulate Expression of CLE, KNOX1, and GRF Family Genes in Nicotiana tabacum | 2017 | Plant molecular biology, tobacco | Preclinical only | PMID DOI |
| Bronchogen | Peptides tissue-specifically stimulate cell differentiation during their aging | 2012 | Organotypic and cell culture across several tissue types | Preclinical only | PMID DOI |
| Buserelin | Treatment with the gonadotrophin-releasing hormone antagonist ganirelix in women undergoing ovarian stimulation with recombinant follicle stimulating hormone is effective, safe and convenient: results of a controlled, randomized, multicentre trial | 2000 | Multicentre randomised controlled non-inferiority trial, 730 women randomised 2:1, ganirelix versus intranasal buserelin long protocol | PMID | |
| Buserelin | Ovarian stimulation with HMG: results of a prospective randomized phase III European study comparing the luteinizing hormone-releasing hormone (LHRH)-antagonist cetrorelix and the LHRH-agonist buserelin | 2000 | Prospective randomised phase 3 European trial, cetrorelix versus buserelin long protocol with human menopausal gonadotrophin | PMID | |
| Buserelin | Maximum androgen blockade using LHRH agonist buserelin in combination with short-term (two weeks) or long-term (continuous) cyproterone acetate is not superior to standard androgen deprivation in the treatment of advanced prostate cancer | 1998 | Randomised controlled trial of buserelin with short-term versus continuous cyproterone acetate in advanced prostate cancer | PMID | |
| Buserelin | Relative effectiveness and cost-effectiveness of methods of androgen suppression in the treatment of advanced prostate cancer | 1999 | Systematic review and meta-analysis of randomised androgen suppression trials | PMID | |
| Cagrilintide | Once-weekly cagrilintide for weight management in people with overweight and obesity: a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial | 2021 | Randomised, double-blind, placebo- and active-controlled phase 2 dose-finding trial, n=706, 26 weeks | Mixed evidence | PMID DOI Trial |
| Cagrilintide | Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2.4 mg for weight management: a randomised, controlled, phase 1b trial | 2021 | Randomised, placebo-controlled phase 1b trial, n=95, 20 weeks | Limited evidence | PMID DOI |
| Cagrilintide | Coadministered Cagrilintide and Semaglutide in Adults with Overweight or Obesity | 2025 | Randomised, double-blind, placebo-controlled phase 3 trial, n=3,417, 68 weeks | High-quality evidence | PMID DOI |
| Cagrilintide | Cagrilintide-Semaglutide in Adults with Overweight or Obesity and Type 2 Diabetes | 2025 | Randomised, double-blind, placebo-controlled phase 3 trial, n=1,206, randomised 3:1 to combination or placebo, 68 weeks | High-quality evidence | PMID DOI |
| Cagrilintide | Cagrilintide lowers bodyweight through brain amylin receptors 1 and 3 | 2025 | Preclinical receptor pharmacology and rodent knockout studies | Preclinical only | PMID DOI |
| Calcitonin gene-related peptide | Alternative RNA processing in calcitonin gene expression generates mRNAs encoding different polypeptide products | 1982 | Molecular biology, tissue-specific RNA processing analysis | PMID | |
| Calcitonin gene-related peptide | CGRP may play a causative role in migraine | 2002 | Human provocation study with intravenous CGRP infusion | PMID | |
| Calcitonin gene-related peptide | A Controlled Trial of Erenumab for Episodic Migraine | 2017 | Phase 3 randomised double-blind placebo-controlled trial over six months (STRIVE) | PMID | |
| Calcitonin gene-related peptide | Ubrogepant for the Treatment of Migraine | 2019 | Phase 3 randomised double-blind placebo-controlled acute treatment trial | PMID | |
| Calcitonin gene-related peptide | Rimegepant, an Oral Calcitonin Gene-Related Peptide Receptor Antagonist, for Migraine | 2019 | Phase 3 randomised double-blind placebo-controlled trial | PMID | |
| Calcitonin gene-related peptide | Atogepant for the Preventive Treatment of Migraine | 2021 | Phase 3 randomised double-blind placebo-controlled 12-week prevention trial (ADVANCE) | PMID | |
| Cardiogen | Interaction of short peptides with FITC-labeled wheat histones and their complexes with deoxyribooligonucleotides | 2013 | In vitro fluorescence quenching, six short peptides against wheat histones H1, H2B, H3 and H4 and histone-oligonucleotide complexes | Preclinical only | PMID DOI |
| Cardiogen | Feasibility of Transport of 26 Biologically Active Ultrashort Peptides via LAT and PEPT Family Transporters | 2023 | In silico molecular modelling and docking against LAT1, LAT2 and PEPT1 transporters | Preclinical only | PMID DOI |
| Cardiogen | Peptides tissue-specifically stimulate cell differentiation during their aging | 2012 | Organotypic and cell culture of several tissues with short peptides | Preclinical only | PMID DOI |
| Cardiogen | The tissue-specific effect of synthetic peptides-biologic regulators in organotypic tissues culture in young and old rats | 2006 | Organotypic tissue culture, young and old rats, Russian language | Preclinical only | PMID |
| carfilzomib | A phase 2 study of single-agent carfilzomib (PX-171-003-A1) in patients with relapsed and refractory multiple myeloma | 2012 | Open-label single-arm phase 2, 266 patients with relapsed and refractory myeloma, median five prior lines | PMID DOI | |
| carfilzomib | Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma | 2015 | Randomised open-label phase 3 (ASPIRE), 792 patients with one to three prior therapies | PMID DOI | |
| carfilzomib | Carfilzomib and dexamethasone versus bortezomib and dexamethasone for patients with relapsed or refractory multiple myeloma (ENDEAVOR): a randomised, phase 3, open-label, multicentre study | 2016 | Randomised open-label phase 3 head-to-head comparison of two proteasome inhibitors, 929 patients | PMID DOI | |
| carfilzomib | Carfilzomib or bortezomib in relapsed or refractory multiple myeloma (ENDEAVOR): an interim overall survival analysis of an open-label, randomised, phase 3 trial | 2017 | Pre-specified interim overall survival analysis of the ENDEAVOR phase 3 trial | PMID DOI | |
| carfilzomib | Improvement in overall survival with carfilzomib, lenalidomide, and dexamethasone in patients with relapsed or refractory multiple myeloma | 2018 | Final overall survival analysis of the ASPIRE phase 3 trial | PMID DOI | |
| carfilzomib | Carfilzomib or bortezomib with melphalan-prednisone for transplant-ineligible patients with newly diagnosed multiple myeloma | 2019 | Randomised open-label phase 3 (CLARION), 955 newly diagnosed transplant-ineligible patients randomised 1:1 to carfilzomib or bortezomib with melphalan and prednisone | PMID DOI | |
| Carperitide | Effects of carperitide on the long-term prognosis of patients with acute decompensated chronic heart failure: the PROTECT multicenter randomized controlled study | 2008 | Multicentre randomised controlled study; 49 patients with acute decompensated heart failure, low-dose carperitide infusion (n=26) versus standard treatment (n=23), 18-month follow-up | PMID DOI | |
| Carperitide | Carperitide is associated with increased in-hospital mortality in acute heart failure: a propensity score-matched analysis | 2015 | Multicentre Japanese observational cohort; 1,037 patients with acute heart failure, 402 (38.7%) treated with carperitide, 367 propensity-matched pairs | PMID DOI | |
| Carperitide | Effect of carperitide on clinical outcomes among patients with acute heart failure: a meta-analysis of randomized and propensity-matched studies | 2025 | Systematic review and meta-analysis of 9 studies (4 randomised controlled trials, 5 propensity score-matched cohorts) in acute heart failure | PMID DOI | |
| Cerebrolysin | Cerebrolysin in patients with acute ischemic stroke in Asia: results of a double-blind, placebo-controlled randomized trial (CASTA) | 2012 | Randomised, double-blind, placebo-controlled multicentre trial, n=1,070 (529 Cerebrolysin, 541 placebo); 30 mL daily intravenous infusion for 10 days added to aspirin, randomised within 12 hours of onset, 90-day follow-up; primary endpoint a combined global directional test of mRS, Barthel Index and NIHSS | Mixed evidence | PMID DOI Trial |
| Cerebrolysin | Cerebrolysin and Recovery After Stroke (CARS): A Randomized, Placebo-Controlled, Double-Blind, Multicenter Trial | 2016 | Prospective, randomised, double-blind, placebo-controlled, multicentre parallel-group trial in early rehabilitation; 30 mL daily for 21 days starting 24-72 hours after stroke onset alongside a standardised rehabilitation programme; primary endpoint Action Research Arm Test at day 90. Sample size not stated in the indexed abstract. | Mixed evidence | PMID DOI Trial |
| Cerebrolysin | Cerebrolysin for acute ischaemic stroke | 2023 | Cochrane systematic review and meta-analysis (CD007026.pub7); 7 RCTs, 1,773 participants; 6 trials and 1,689 participants for all-cause mortality | High-quality evidence | PMID DOI |
| Cerebrolysin | Cerebrolysin for vascular dementia | 2019 | Cochrane systematic review and meta-analysis (CD008900.pub3); 6 RCTs, 597 participants; follow-up 15 days to 3 years | Mixed evidence | PMID DOI |
| Cerebrolysin | A 24-week, double-blind, placebo-controlled study of three dosages of Cerebrolysin in patients with mild to moderate Alzheimer's disease | 2006 | 24-week randomised, double-blind, placebo-controlled dose-ranging study, n=279 (69 at 10 mL, 70 at 30 mL, 71 at 60 mL, 69 placebo); intravenous infusions 5 days weekly for 4 weeks then twice weekly for 8 weeks; ADAS-cog and CIBIC+ endpoints | Mixed evidence | PMID DOI |
| Cerebrolysin | A 28-week, double-blind, placebo-controlled study with Cerebrolysin in patients with mild to moderate Alzheimer's disease | 2001 | 28-week randomised, double-blind, placebo-controlled multicentre parallel-group trial, n=149 (76 Cerebrolysin, 73 placebo); two 4-week courses of 30 mL intravenously 5 days weekly separated by a 2-month therapy-free interval | Mixed evidence | PMID DOI |
| Cerebrolysin | Cerebrolysin in Alzheimer's disease: a randomized, double-blind, placebo-controlled trial with a neurotrophic agent | 2002 | Multicentre randomised, double-blind, placebo-controlled parallel-group trial, n=192 (97 Cerebrolysin, 95 placebo); 30 mL intravenously 5 days weekly for 4 weeks; ADAS-Cog and CIBIC+ at 4, 12 and 24 weeks | Mixed evidence | PMID DOI |
| Cerebrolysin | Safety profile of Cerebrolysin: clinical experience from dementia and stroke trials | 2012 | Review of pooled safety data from dementia and stroke trials | Mixed evidence | PMID DOI |
| Cerebrolysin | Randomized, placebo-controlled, double-blind, pilot trial to investigate safety and efficacy of Cerebrolysin in patients with aneurysmal subarachnoid hemorrhage | 2020 | Randomised, double-blind, placebo-controlled, single-centre parallel-group pilot trial, n=50 (25 per arm); 30 mL daily for 14 days; primary endpoint favourable Extended Glasgow Outcome Scale (5-8) at six months | Mixed evidence | PMID DOI Trial |
| Cetrorelix | Ovarian stimulation with HMG: results of a prospective randomized phase III European study comparing the luteinizing hormone-releasing hormone (LHRH)-antagonist cetrorelix and the LHRH-agonist buserelin | 2000 | Prospective randomised phase 3 multicentre European trial, cetrorelix versus buserelin long protocol with human menopausal gonadotrophin | PMID | |
| Cetrorelix | Significant reduction of the incidence of ovarian hyperstimulation syndrome (OHSS) by using the LHRH antagonist Cetrorelix (Cetrotide) in controlled ovarian stimulation for assisted reproduction | 2000 | Comparative analysis of ovarian hyperstimulation syndrome incidence across cetrorelix and agonist protocol cohorts | PMID | |
| Cetrorelix | Gonadotrophin-releasing hormone antagonists for assisted reproductive technology | 2016 | Cochrane systematic review and meta-analysis of randomised trials comparing GnRH antagonist with agonist long protocols | PMID DOI | |
| Cholecystokinin | C-terminal octapeptide of cholecystokinin decreases food intake in man | 1981 | Controlled human infusion study, 12 lean men | PMID | |
| Cholecystokinin | C-terminal octapeptide of cholecystokinin decreases food intake in obese men | 1982 | Controlled human infusion study, 8 obese men | PMID | |
| Cholecystokinin | Satiety effects of a physiological dose of cholecystokinin in humans | 1995 | Crossover infusion study in obese and lean women | PMID DOI | |
| Cholecystokinin | Stimulation of cholecystokinin-A receptors with GI181771X does not cause weight loss in overweight or obese patients | 2008 | 24-week randomised, double-blind, placebo-controlled trial of a selective CCK1 agonist with hypocaloric diet, with prospective gallbladder and pancreatic imaging | PMID | |
| Cholecystokinin | Role of cholecystokinin in satiation: a systematic review and meta-analysis | 2023 | PRISMA-2020 systematic review and meta-analysis of human studies of exogenous CCK or analogues on satiation and body weight, across five databases | PMID DOI | |
| Cibinetide (ARA-290) | ARA 290 improves symptoms in patients with sarcoidosis-associated small nerve fiber loss and increases corneal nerve fiber density | 2013 | Blinded, placebo-controlled randomised trial; 28 days daily subcutaneous administration | Mixed evidence | PMID DOI |
| Cibinetide (ARA-290) | Cibinetide Improves Corneal Nerve Fiber Abundance in Patients With Sarcoidosis-Associated Small Nerve Fiber Loss and Neuropathic Pain | 2017 | Phase 2b randomised placebo-controlled, 28 days, 64 subjects, doses of 1, 4 and 8 mg/day | Mixed evidence | PMID DOI Trial |
| Cibinetide (ARA-290) | ARA 290, a nonerythropoietic peptide engineered from erythropoietin, improves metabolic control and neuropathic symptoms in patients with type 2 diabetes | 2015 | Phase 2 randomised placebo-controlled; 4 mg daily self-administered subcutaneously for 28 days with 28 days follow-up | Mixed evidence | PMID DOI |
| Cibinetide (ARA-290) | A Phase 2 Clinical Trial on the Use of Cibinetide for the Treatment of Diabetic Macular Edema | 2020 | Phase 2 clinical trial in diabetic macular oedema | Mixed evidence | PMID DOI |
| Cibinetide (ARA-290) | ARA 290, a peptide derived from the tertiary structure of erythropoietin, produces long-term relief of neuropathic pain coupled with suppression of the spinal microglia response | 2014 | Rodent neuropathic pain model | Preclinical only | PMID DOI |
| Cibinetide (ARA-290) | ARA 290 relieves pathophysiological pain by targeting TRPV1 channel: Integration between immune system and nociception | 2016 | In vitro and rodent nociception studies | Preclinical only | PMID DOI |
| ciclosporin | A randomized clinical trial of cyclosporine in cadaveric renal transplantation | 1983 | Multicentre randomised controlled trial, 209 recipients of cadaveric renal transplants, ciclosporin plus prednisone versus azathioprine plus prednisone | PMID | |
| ciclosporin | Cyclosporin in cadaveric renal transplantation: one-year follow-up of a multicentre trial | 1983 | Multicentre randomised controlled trial across eight European centres, 232 recipients of cadaveric renal allografts | PMID | |
| ciclosporin | A randomized clinical trial of cyclosporine in cadaveric renal transplantation. Analysis at three years | 1986 | Three-year analysis of the Canadian randomised trial, 291 recipients (142 ciclosporin plus prednisone, 149 control immunosuppression) | PMID DOI | |
| ciclosporin | Cyclosporine for plaque-type psoriasis. Results of a multidose, double-blind trial | 1991 | Randomised double-blind vehicle-controlled dose-ranging trial, 85 patients with severe plaque psoriasis, 16 weeks | PMID DOI | |
| ciclosporin | Preliminary report: cyclosporin in treatment of severe active ulcerative colitis | 1990 | Uncontrolled prospective study, 32 patients with active ulcerative colitis refractory to corticosteroid therapy | PMID | |
| ciclosporin | Cyclosporine in severe ulcerative colitis refractory to steroid therapy | 1994 | Randomised double-blind placebo-controlled trial, 20 patients (11 ciclosporin, 9 placebo) with severe ulcerative colitis unimproved after at least seven days of intravenous corticosteroids | PMID DOI | |
| ciclosporin | Two multicenter, randomized studies of the efficacy and safety of cyclosporine ophthalmic emulsion in moderate to severe dry eye disease | 2000 | Two identical randomised vehicle-controlled multicentre trials, 877 patients, six months | PMID | |
| CJC-1293 | Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS | 2016 | Analytical method development and validation in human plasma, with supporting animal administration samples | PMID DOI | |
| CJC-1293 | Online large volume sample stacking preconcentration and separation of enantiomeric GHRH analogs by capillary electrophoresis | 2023 | Analytical separation method development using dimethyl-beta-cyclodextrin as chiral selector, applied to urine | PMID DOI | |
| CJC-1293 | Expanded test method for peptides >2 kDa employing immunoaffinity purification and LC-HRMS/MS | 2015 | Analytical method expansion for doping control of peptides between 2 and 12 kilodaltons in blood and urine | PMID DOI | |
| CJC-1293 | In-house standards derived from doping peptides: Enzymatic and serum stability and degradation profile of GHRP and GHRH-related peptides | 2023 | In vitro enzymatic and human serum stability and degradation profiling of six synthesised GHRP and GHRH-related peptides | PMID DOI | |
| CJC-1295 (with DAC) | Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults | 2006 | Two randomised, double-blind, placebo-controlled ascending-dose trials in healthy adults, 28 and 49 days; biomarker endpoints only | Limited evidence | PMID DOI |
| CJC-1295 (with DAC) | Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog | 2006 | Frequent-sampling pharmacodynamic study in healthy adults after a single injection | Limited evidence | PMID DOI |
| CJC-1295 (with DAC) | Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse | 2006 | Controlled animal study in GHRH-knockout mice, dosing intervals of 24, 48 and 72 hours | Preclinical only | PMID DOI |
| CJC-1295 without DAC (modified GRF 1-29) | Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults | 2006 | Two randomised, double-blind, placebo-controlled ascending-dose trials in healthy adults; studied the albumin-conjugated (DAC) molecule only | Limited evidence | PMID DOI |
| CJC-1295 without DAC (modified GRF 1-29) | Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency | 1999 | Narrative review of clinical data on unmodified GRF(1-29) | Limited evidence | PMID DOI |
| Colistin (colistimethate sodium) | Colistin alone versus colistin plus meropenem for treatment of severe infections caused by carbapenem-resistant Gram-negative bacteria: an open-label, randomised controlled trial | 2018 | Multicentre open-label randomised controlled trial; 406 patients with severe carbapenem-resistant Gram-negative infection | PMID DOI | |
| Colistin (colistimethate sodium) | Multicentre open-label randomised controlled trial to compare colistin alone with colistin plus meropenem for the treatment of severe infections caused by carbapenem-resistant Gram-negative infections (AIDA): a study protocol | 2016 | Published trial protocol | PMID DOI | |
| Colistin (colistimethate sodium) | Colistin Monotherapy versus Combination Therapy for Carbapenem-Resistant Organisms | 2023 | Multicentre double-blind randomised controlled trial (OVERCOME); 423 randomised patients with pneumonia or bloodstream infection caused by extensively drug-resistant organisms, predominantly Acinetobacter baumannii | PMID DOI | |
| Colistin (colistimethate sodium) | Polymyxin-containing medicines: Article 31 referral, European Medicines Agency review of colistin and colistimethate sodium | 2014 | Regulatory safety and efficacy review by the EMA Committee for Medicinal Products for Human Use | none | |
| Colistin (colistimethate sodium) | Carbapenem-resistant Enterobacterales (CRE) acquisition and molecular characterization following colistin monotherapy and colistin-meropenem combination therapy: findings from the AIDA randomized trial | 2025 | Secondary microbiological analysis of the AIDA randomised trial cohort (volume 14, article 133) | PMID DOI | |
| Colivelin | Development of a femtomolar-acting humanin derivative named colivelin by attaching activity-dependent neurotrophic factor to its N terminus: characterization of colivelin-mediated neuroprotection against Alzheimer's disease-relevant insults in vitro and in vivo | 2005 | In vitro neuroprotection assays plus in vivo mouse memory impairment model | Preclinical only | PMID DOI |
| Colivelin | Colivelin prolongs survival of an ALS model mouse | 2006 | Amyotrophic lateral sclerosis model mouse survival study | Preclinical only | PMID DOI |
| Colivelin | Nasal Colivelin treatment ameliorates memory impairment related to Alzheimer's disease | 2008 | Intranasal administration in a rodent Alzheimer-related memory impairment model | Preclinical only | PMID DOI |
| Colivelin | Colivelin ameliorates amyloid beta peptide-induced impairments in spatial memory, synaptic plasticity, and calcium homeostasis in rats | 2015 | Amyloid-beta-treated rats with behavioural, electrophysiological and calcium imaging endpoints | Preclinical only | PMID DOI |
| Colivelin | Colivelin Ameliorates Impairments in Cognitive Behaviors and Synaptic Plasticity in APP/PS1 Transgenic Mice | 2017 | APP/PS1 transgenic mouse model | Preclinical only | PMID DOI |
| Colivelin | Colivelin Rescues Ischemic Neuron and Axons Involving JAK/STAT3 Signaling Pathway | 2019 | Cerebral ischaemia model with neuronal and axonal endpoints | Preclinical only | PMID DOI |
| Colivelin | Colivelin, a synthetic derivative of humanin, ameliorates endothelial injury and glycocalyx shedding after sepsis in mice | 2022 | Murine sepsis model with endothelial and glycocalyx endpoints | Preclinical only | PMID DOI |
| Colivelin | Humanin and colivelin: neuronal-death-suppressing peptides for Alzheimer's disease and amyotrophic lateral sclerosis | 2006 | Review of humanin and colivelin biology and receptor pharmacology | Preclinical only | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Effects of topical copper tripeptide complex on CO2 laser-resurfaced skin | 2006 | Randomised controlled trial after circumoral CO2 laser resurfacing, with blinded evaluators and computerised erythema analysis; 13 patients completed | Limited evidence | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Stimulation of sulfated glycosaminoglycan synthesis by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+ | 1992 | In vitro and in vivo rodent connective tissue | Preclinical only | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Effect of tripeptide-copper complexes on the process of skin wound healing and on cultured fibroblasts | 1995 | Rodent skin wound model plus cultured fibroblasts | Preclinical only | PMID |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Human skin retention and penetration of a copper tripeptide in vitro as function of skin layer towards anti-inflammatory therapy | 2010 | In vitro human skin penetration study by skin layer | Preclinical only | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | The human tri-peptide GHK and tissue remodeling | 2008 | Narrative review | Preclinical only | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | The human tripeptide GHK-Cu in prevention of oxidative stress and degenerative conditions of aging: implications for cognitive health | 2012 | Narrative review and hypothesis paper | Preclinical only | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Enhanced healing of ulcers in patients with diabetes by topical treatment with glycyl-l-histidyl-l-lysine copper | 1994 | Multicentre, randomised, evaluator-blinded, placebo-controlled trial in diabetic neuropathic ulcers, with sharp debridement at entry, daily metered dosing, standardised pressure-relieving footwear and patient education | Mixed evidence | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Skin care benefits of copper peptide containing facial cream (and companion eye cream study) | 2002 | Reported as a 12-week study of a GHK-Cu facial cream in 71 women with photoaged skin, with a companion eye cream study in 41 women | Limited evidence | none |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | GHK Peptide as a Natural Modulator of Multiple Cellular Pathways in Skin Regeneration | 2015 | Narrative review of GHK and GHK-Cu cellular and molecular actions | Preclinical only | PMID DOI |
| Copper(II) glycyl-L-histidyl-L-lysine (GHK-Cu) | Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data | 2018 | Review of gene-expression and transcriptomic data relating to GHK and GHK-Cu | Preclinical only | PMID DOI |
| Cortagen | Effect of tetrapeptide cortagen on regeneration of sciatic nerve | 2000 | Rat sciatic nerve crush injury model | Preclinical only | PMID |
| Cortagen | The delayed effect of cortagen on the restoration of injured nerve function | 2002 | Rat peripheral nerve injury model, delayed assessment | Preclinical only | PMID DOI |
| Cortagen | Elucidation of the effect of brain cortex tetrapeptide Cortagen on gene expression in mouse heart by microarray | 2004 | Microarray transcriptomic profiling, mouse heart | Preclinical only | PMID |
| Cortagen | Effects of bioactive tetrapeptides on free-radical processes | 2007 | Rat, injections of Cortagen and Epitalon, serum and cerebral cortex measurements | Preclinical only | PMID DOI |
| Cortagen | Cortexin and cortagen as correcting agents in functional and metabolic disorders in the brain in chronic ischemia | 2011 | Animal model of chronic cerebral ischaemia, Russian language | Preclinical only | PMID |
| Cortagen | Effects of short peptides on lymphocyte chromatin in senile subjects | 2004 | Ex vivo lymphocyte chromatin analysis from elderly donors | Preclinical only | PMID DOI |
| Corticorelin | Petrosal sinus sampling with and without corticotropin-releasing hormone for the differential diagnosis of Cushing's syndrome | 1991 | Prospective study in 281 patients with Cushing's syndrome; bilateral inferior petrosal sinus sampling was successful in 278, of whom 262 underwent sampling before and after ovine CRH. Diagnosis was surgically confirmed in 246 (215 Cushing's disease, 20 ectopic ACTH, 11 primary adrenal disease) | PMID DOI | |
| Corticorelin | The ovine corticotropin-releasing hormone stimulation test and the dexamethasone suppression test in the differential diagnosis of Cushing's syndrome | 1986 | Prospective comparison of the ovine CRH stimulation test with the standard dexamethasone suppression test in 41 patients with ACTH-dependent hypercortisolism (33 Cushing's disease, 8 ectopic ACTH) | PMID DOI | |
| Corticorelin | A simplified morning ovine corticotropin-releasing hormone stimulation test for the differential diagnosis of adrenocorticotropin-dependent Cushing's syndrome | 1993 | Prospective evaluation of a simplified morning protocol for the ovine CRH stimulation test in ACTH-dependent Cushing's syndrome | PMID DOI | |
| Corticorelin | Ovine CRH Stimulation and 8 mg Dexamethasone Suppression Tests in 323 Patients With ACTH-Dependent Cushing's Syndrome | 2023 | Retrospective review at a tertiary referral centre of 323 patients with ACTH-dependent Cushing's syndrome (including 78 with ectopic ACTH) who underwent both the ovine CRH stimulation test and the 8 mg high-dose dexamethasone suppression test between 1986 and 2019 | PMID DOI | |
| Corticotropin (ACTH 1-39) | High-dose corticotropin (ACTH) versus prednisone for infantile spasms: a prospective, randomized, blinded study | 1996 | Prospective, randomised, single-blind trial, n=29 infants (15 corticotropin, 14 prednisone), median age 6 months; 2-week course of repository corticotropin 150 U/m2/day versus prednisone 2 mg/kg/day | Mixed evidence | PMID |
| Corticotropin (ACTH 1-39) | The United Kingdom Infantile Spasms Study comparing vigabatrin with prednisolone or tetracosactide at 14 days: a multicentre, randomised controlled trial | 2004 | Multicentre randomised controlled trial, n=107 infants (vigabatrin n=52; hormonal treatment n=55, comprising prednisolone n=30 and tetracosactide n=25) | High-quality evidence | PMID DOI |
| Corticotropin (ACTH 1-39) | Repository Corticotropin Injection for Active Rheumatoid Arthritis Despite Aggressive Treatment: A Randomized Controlled Withdrawal Trial | 2020 | 12-week open-label lead-in followed by a 12-week double-blind randomised withdrawal period; 259 enrolled, 154 responders randomised (77 per arm), 127 completed | Mixed evidence | PMID DOI |
| Corticotropin (ACTH 1-39) | Repository Corticotropin Injection for Persistently Active Systemic Lupus Erythematosus: Results from a Phase 4, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial | 2020 | Phase 4 multicentre randomised, double-blind, placebo-controlled trial; 169 patients in the modified intent-to-treat population (84 active, 85 placebo) | Mixed evidence | PMID DOI |
| Corticotropin (ACTH 1-39) | A Randomized Prospective Trial Comparing Repository Corticotropin Injection and Intravenous Methylprednisolone for Neuroprotection in Acute Optic Neuritis | 2023 | Randomised prospective comparative trial, n=37 (19 repository corticotropin, 18 intravenous methylprednisolone), 6-month follow-up | Mixed evidence | PMID DOI |
| Crystagen (Glu-Asp-Pro) | [Molecular aspects of immunoprotective activity of peptides in spleen during the ageing process] | 2014 | Russian-language laboratory study of peptide effects on spleen tissue during ageing, examining vilon, thymogen, crystagen and R-1; volume 27(1):224-228 | Preclinical only | PMID |
| Crystagen (Glu-Asp-Pro) | The Use of Thymalin for Immunocorrection and Molecular Aspects of Biological Activity | 2021 | Narrative review by the developing group; identifies crystagen as EDP (Glu-Asp-Pro), one of the active short peptides within thymalin; volume 11(4):377-382 | Limited evidence | DOI |
| Crystagen (Glu-Asp-Pro) | Transport of Biologically Active Ultrashort Peptides Using POT and LAT Carriers | 2022 | Review and modelling of proton-coupled oligopeptide transporter and large neutral amino acid transporter mediated uptake of ultrashort peptides (2-7 residues); volume 23(14):7733 | Preclinical only | PMID DOI |
| Daptomycin | The safety and efficacy of daptomycin for the treatment of complicated skin and skin-structure infections | 2004 | Pooled analysis of two randomised, investigator-blinded, multicentre non-inferiority trials; 1092 patients enrolled, 902 clinically evaluable | PMID | |
| Daptomycin | Daptomycin versus standard therapy for bacteremia and endocarditis caused by Staphylococcus aureus | 2006 | Open-label randomised controlled non-inferiority trial; 246 patients (124 daptomycin, 122 standard therapy) | PMID DOI | |
| Daptomycin | Effects of prior effective therapy on the efficacy of daptomycin and ceftriaxone for the treatment of community-acquired pneumonia | 2008 | Combined analysis of two phase 3 randomised, double-blind trials in hospitalised adults with community-acquired pneumonia; 834 patients in the intention-to-treat population (413 daptomycin, 421 ceftriaxone), 740 clinically evaluable | PMID DOI | |
| Daptomycin | An open-label, pragmatic, randomized controlled clinical trial to evaluate the comparative effectiveness of daptomycin versus vancomycin for the treatment of complicated skin and skin structure infection | 2015 | Pragmatic open-label randomised controlled trial | PMID DOI | |
| Daptomycin | Safety and efficacy of daptomycin as first-line treatment for complicated skin and soft tissue infections in elderly patients: an open-label, multicentre, randomized phase IIIb trial | 2013 | Open-label multicentre randomised phase 3b trial in elderly patients | PMID DOI | |
| Degarelix | The efficacy and safety of degarelix: a 12-month, comparative, randomized, open-label, parallel-group phase III study in patients with prostate cancer | 2008 | Randomised open-label parallel-group phase 3 trial (CS21), 610 men, degarelix versus leuprorelin 7.5 mg monthly over 12 months | PMID | |
| Degarelix | Additional analysis of the secondary end point of biochemical recurrence rate in a phase 3 trial (CS21) comparing degarelix 80 mg versus leuprolide in prostate cancer patients segmented by baseline characteristics | 2010 | Prespecified and exploratory subgroup analysis of the CS21 randomised trial | PMID | |
| Degarelix | Cardiovascular Safety of Degarelix Versus Leuprolide in Patients With Prostate Cancer: The Primary Results of the PRONOUNCE Randomized Trial | 2021 | Randomised open-label cardiovascular outcomes trial, 545 men with prostate cancer and established cardiovascular disease | PMID Trial | |
| Delta sleep-inducing peptide (DSIP) | Synthetic delta-sleep-inducing peptide improves sleep in insomniacs | 1981 | Short clinical report published as a Lancet letter; PubMed indexes it with the Clinical Trial and Randomized Controlled Trial publication types, but no methods detail is available in the indexed record | Limited evidence | PMID DOI |
| Delta sleep-inducing peptide (DSIP) | Efficacy of DSIP to normalize sleep in middle-aged and elderly chronic insomniacs | 1986 | Sleep-laboratory study in 18 chronic psychophysiological insomniacs stratified by age (middle-aged 29-59, elderly 60-83); six doses of 30 nmol/kg intravenously over one week with a one-week follow-up. No placebo or control condition is described in the abstract. | Limited evidence | PMID DOI |
| Delta sleep-inducing peptide (DSIP) | Study of delta sleep-inducing peptide efficacy in improving sleep on short-term administration to chronic insomniacs | 1987 | Double-blind crossover polysomnographic study, 25 nmol/kg intravenously or placebo over four nights in chronic insomniacs; sample size not stated in the indexed abstract | Limited evidence | PMID |
| Delta sleep-inducing peptide (DSIP) | The influence of synthetic DSIP (delta-sleep-inducing-peptide) on disturbed human sleep | 1981 | Human sleep study in disturbed sleep; indexed as a clinical trial | Limited evidence | PMID DOI |
| Delta sleep-inducing peptide (DSIP) | Delta-sleep-inducing peptide (DSIP): a review | 1984 | Comprehensive review of DSIP biology, distribution and pharmacokinetics | Preclinical only | PMID DOI |
| Delta sleep-inducing peptide (DSIP) | Delta-sleep-inducing peptide reduces CRF-induced corticosterone release | 1985 | Animal neuroendocrine study | Preclinical only | PMID DOI |
| Delta sleep-inducing peptide (DSIP) | Delta-sleep-inducing peptide (DSIP): an update | 1986 | Review updating the DSIP literature | Preclinical only | PMID DOI |
| Delta sleep-inducing peptide (DSIP) | Delta sleep-inducing peptide in opioid detoxification | 1997 | Case report published as a letter to the editor; two pages, no controlled comparison | Limited evidence | PMID DOI |
| Dermorphin | Amino acid composition and sequence of dermorphin, a novel opiate-like peptide from the skin of Phyllomedusa sauvagei | 1981 | Isolation and structural characterisation from methanol extracts of frog skin | Preclinical only | PMID DOI |
| Dermorphin | Pharmacological data on dermorphins, a new class of potent opioid peptides from amphibian skin | 1981 | In vitro isolated tissue pharmacology (guinea-pig ileum, mouse vas deferens) plus in vivo antinociception and tolerance/dependence studies in mice and rats | Preclinical only | PMID DOI |
| Dermorphin | Intrathecal dermorphine in postoperative analgesia | 1985 | Prospective randomised double-blind study, n=150 consecutive patients after elective surgery; three arms: intrathecal dermorphin 20 micrograms, intrathecal morphine 500 micrograms, or routine intramuscular pentazocine 30 mg | Limited evidence | PMID DOI |
| Dermorphin | Rediscovery of old drugs: the forgotten case of dermorphin for postoperative pain and palliation | 2018 | Historical analysis and drug-repurposing argument reviewing the dermorphin literature | Limited evidence | PMID DOI |
| Dermorphin | Dermorphin: A Missed Palliative Care Opportunity for Intrathecal Therapy in Oncological Patients? | 2019 | Short commentary (three pages) on the human intrathecal dermorphin literature | Limited evidence | PMID DOI |
| Dermorphin | Detection, quantification, and identification of dermorphin in equine plasma and urine by LC-MS/MS for doping control | 2013 | Analytical method development and validation using research horse samples and official post-race specimens | Preclinical only | PMID DOI |
| des(1-3)IGF-1 | Des(1-3)IGF-I: a truncated form of insulin-like growth factor-I | 1996 | Narrative review of the biochemistry, occurrence and biological activity of des(1-3)IGF-1 | Preclinical only | PMID DOI |
| des(1-3)IGF-1 | Plasma clearance and tissue distribution of labelled insulin-like growth factor-I (IGF-I), IGF-II and des(1-3)IGF-I in rats | 1991 | Radiolabelled tracer pharmacokinetic and tissue-distribution study in rats | Preclinical only | PMID DOI |
| des(1-3)IGF-1 | Increased weight gain, nitrogen retention and muscle protein synthesis following treatment of diabetic rats with insulin-like growth factor (IGF)-I and des(1-3)IGF-I | 1991 | Seven-day continuous infusion study in streptozotocin-diabetic rats comparing hGH, IGF-1, des(1-3)IGF-1 and insulin | Preclinical only | PMID DOI |
| des(1-3)IGF-1 | IGF-I and the truncated analogue des-(1-3)IGF-I enhance growth in rats after gut resection | 1991 | Controlled infusion study in rats following gut resection | Preclinical only | PMID DOI |
| des(1-3)IGF-1 | Enhanced potency of truncated insulin-like growth factor-I (des(1-3)IGF-I) relative to IGF-I in lit/lit mice | 1990 | Comparative growth study in growth-hormone-deficient lit/lit mice | Preclinical only | PMID DOI |
| des(1-3)IGF-1 | Novel recombinant fusion protein analogues of insulin-like growth factor (IGF)-I indicate the relative importance of IGF-binding protein and receptor binding for enhanced biological potency | 1992 | Comparative in vitro potency and binding study across N-terminally modified IGF-1 analogues and des(1-3)IGF-I | Preclinical only | PMID DOI |
| Desirudin | Prevention of thromboembolism with use of recombinant hirudin. Results of a double-blind, multicenter trial comparing the efficacy of desirudin with that of unfractionated heparin in patients having a total hip replacement | 1997 | Double-blind, multicentre randomised trial; 445 patients undergoing total hip replacement randomised (225 desirudin, 220 unfractionated heparin), 351 evaluable, with bilateral venography as the endpoint | PMID DOI | |
| Desirudin | A comparison of recombinant hirudin with a low-molecular-weight heparin to prevent thromboembolic complications after total hip replacement | 1997 | Double-blind, multicentre randomised trial; 2,079 patients randomised undergoing total hip replacement (1,587 in the primary efficacy analysis), desirudin versus enoxaparin, venographic endpoint | PMID DOI | |
| Desirudin | Antihirudin antibodies following low-dose subcutaneous treatment with desirudin for thrombosis prophylaxis after hip-replacement surgery: incidence and clinical relevance | 2003 | Prospective immunogenicity analysis in 112 orthopaedic patients receiving subcutaneous desirudin across three dose groups (17 at 10 mg twice daily, 75 at 15 mg twice daily, 20 at 20 mg twice daily) | PMID DOI | |
| Deslorelin | Effect of deslorelin dose in the treatment of central precocious puberty | 1991 | Prospective dose-ranging study in children with central precocious puberty; single-centre, no control group | PMID | |
| Deslorelin | Adult height in precocious puberty after long-term treatment with deslorelin | 1991 | Single-arm longitudinal follow-up of children treated long-term for central precocious puberty | PMID | |
| Deslorelin | Six-year results of spironolactone and testolactone treatment of familial male-limited precocious puberty with addition of deslorelin after central puberty onset | 1999 | Small long-term open-label study in familial male-limited precocious puberty | PMID | |
| Difelikefalin | A phase 3 trial of difelikefalin in hemodialysis patients with pruritus | 2020 | Randomised, double-blind, placebo-controlled phase 3 trial; 378 haemodialysis patients with moderate-to-severe pruritus at 56 US sites (158 difelikefalin, 165 placebo in the analysis), intravenous difelikefalin 0.5 µg/kg or placebo three times weekly for 12 weeks | PMID DOI Trial | |
| Difelikefalin | Efficacy of difelikefalin for the treatment of moderate to severe pruritus in hemodialysis patients: pooled analysis of KALM-1 and KALM-2 phase 3 studies | 2022 | Pooled analysis of two randomised, double-blind, placebo-controlled phase 3 trials; 851 patients randomised (426 difelikefalin, 425 placebo) | PMID DOI | |
| Difelikefalin | Difelikefalin for hemodialysis patients with pruritus in Japan | 2023 | Randomised, double-blind, placebo-controlled trial; 178 Japanese haemodialysis patients (89 difelikefalin, 89 placebo), intravenous difelikefalin 0.5 µg/kg or placebo three times weekly | PMID DOI | |
| Dihexa | Retraction notice to 'The Procognitive and Synaptogenic Effects of Angiotensin IV-Derived Peptides Are Dependent on Activation of the Hepatocyte Growth Factor/c-Met System' | 2025 | Editorial retraction notice withdrawing the 2014 paper (J Pharmacol Exp Ther 2014 Nov;351(2):390-402, doi 10.1124/jpet.114.218735, PMID 25187433) | Preclinical only | PMID DOI |
| Dihexa | Retraction notice to 'Development of Angiotensin IV Analogs as Hepatocyte Growth Factor/Met Modifiers' | 2025 | Editorial retraction notice withdrawing the 2012 paper (J Pharmacol Exp Ther 2012 Mar;340(3):539-48, doi 10.1124/jpet.111.188136, PMID 22129598) | Preclinical only | PMID DOI |
| Dihexa | Retraction notice to 'Mimics of the Dimerization Domain of Hepatocyte Growth Factor Exhibit Anti-Met and Anticancer Activity' | 2025 | Editorial retraction notice withdrawing the 2011 paper (J Pharmacol Exp Ther 2011 Nov;339(2):509-18, doi 10.1124/jpet.111.185694, PMID 21859930) | Preclinical only | PMID DOI |
| Dihexa | Evaluation of metabolically stabilized angiotensin IV analogs as procognitive/antidementia agents | 2013 | Rodent cognition studies (scopolamine-induced deficit and aged-rat models) with synaptogenesis assessment | Preclinical only | PMID DOI |
| Dihexa | The development of small molecule angiotensin IV analogs to treat Alzheimer's and Parkinson's diseases | 2015 | Review of the angiotensin IV analogue programme | Preclinical only | PMID DOI |
| Dihexa | AngIV-Analog Dihexa Rescues Cognitive Impairment and Recovers Memory in the APP/PS1 Mouse via the PI3K/AKT Signaling Pathway | 2021 | APP/PS1 transgenic mouse model of Alzheimer's pathology | Preclinical only | PMID DOI |
| Dihexa | Hepatocyte growth factor mimetic protects lateral line hair cells from aminoglycoside exposure | 2015 | Zebrafish lateral line hair cell protection model | Preclinical only | PMID DOI |
| Dihexa | Effects of an Angiotensin IV Analog on 3-Nitropropionic Acid-Induced Huntington's Disease-Like Symptoms in Rats | 2024 | Rat 3-nitropropionic acid model of Huntington's-like pathology | Preclinical only | PMID DOI |
| Dihexa | Cognitive benefits of angiotensin IV and angiotensin-(1-7): A systematic review of experimental studies | 2018 | Systematic review of experimental (animal) studies | Preclinical only | PMID DOI |
| dipeptide diaminobutyroyl benzylamide diacetate | The effect of a serum containing acetyl hexapeptide-8, dipeptide diaminobutyroyl benzylamide diacetate and gluconolactone on skin biomarkers, wrinkles and skin texture: Ex vivo and clinical studies | 2026 | Ex vivo human skin biomarker study plus two clinical studies (n=50 static wrinkles; n=42 dynamic wrinkles) of a five-active serum | PMID DOI | |
| dipeptide diaminobutyroyl benzylamide diacetate | Molecular properties and structure-function relationships of lethal peptides from venom of Wagler's pit viper, Trimeresurus wagleri | 1992 | Peptide isolation, sequencing and structure-activity analysis | PMID | |
| dipeptide diaminobutyroyl benzylamide diacetate | Waglerin-1 selectively blocks the epsilon form of the muscle nicotinic acetylcholine receptor | 1999 | Electrophysiology and binding studies in receptor-expressing systems | PMID | |
| dipeptide diaminobutyroyl benzylamide diacetate | Identification of residues at the alpha and epsilon subunit interfaces mediating species selectivity of Waglerin-1 for nicotinic acetylcholine receptors | 2002 | Mutagenesis and binding analysis | PMID | |
| dipeptide diaminobutyroyl benzylamide diacetate | Residues in the epsilon subunit of the nicotinic acetylcholine receptor interact to confer selectivity of waglerin-1 for the alpha-epsilon subunit interface site | 2002 | Structural modelling and mutagenesis | PMID | |
| dipeptide diaminobutyroyl benzylamide diacetate | Effects of waglerin-I on neuromuscular transmission of mouse nerve-muscle preparations | 1995 | Ex vivo nerve-muscle preparation | Preclinical only | PMID |
| DNSP-11 | Dopamine neuron stimulating actions of a GDNF propeptide | 2010 | Rat fetal mesencephalic neuron and MN9D cell culture, plus single intranigral injection in normal adult rats and in a 6-hydroxydopamine rat model of Parkinson's disease | Preclinical only | PMID DOI |
| DNSP-11 | Methodology and effects of repeated intranasal delivery of DNSP-11 in a rat model of Parkinson's disease | 2015 | Repeated intranasal administration in a 6-hydroxydopamine rat model | Preclinical only | PMID DOI |
| Dulaglutide | Once-weekly dulaglutide versus once-daily liraglutide in metformin-treated patients with type 2 diabetes (AWARD-6): a randomised, open-label, phase 3, non-inferiority trial | 2014 | 26-week randomised, open-label, active-comparator non-inferiority trial, 599 adults (299 dulaglutide, 300 liraglutide) | PMID DOI | |
| Dulaglutide | Efficacy and safety of dulaglutide added onto pioglitazone and metformin versus exenatide in type 2 diabetes in a randomized controlled trial (AWARD-1) | 2014 | 52-week randomised multicentre trial with a 26-week primary endpoint, allocation 2:2:2:1 to dulaglutide 1.5 mg, dulaglutide 0.75 mg, exenatide 10 micrograms or placebo on background metformin and pioglitazone; approximately 976 adults | PMID DOI | |
| Dulaglutide | Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial | 2019 | Randomised, double-blind, placebo-controlled cardiovascular outcomes trial, 9,901 participants, median follow-up 5.4 years | PMID DOI Trial | |
| Dulaglutide | Efficacy and Safety of Dulaglutide 3.0 mg and 4.5 mg Versus Dulaglutide 1.5 mg in Metformin-Treated Patients With Type 2 Diabetes in a Randomized Controlled Trial (AWARD-11) | 2021 | Randomised, double-blind, parallel-group dose-comparison trial, 1,842 adults, 52 weeks total with the primary efficacy endpoint at 36 weeks | PMID DOI | |
| Dynorphin A | Dynorphin-(1-13), an extraordinarily potent opioid peptide | 1979 | Peptide isolation from porcine pituitary with bioassay | PMID | |
| Dynorphin A | Dynorphin is a specific endogenous ligand of the kappa opioid receptor | 1982 | Receptor binding and functional selectivity studies | PMID DOI | |
| Dynorphin A | The dysphoric component of stress is encoded by activation of the dynorphin kappa-opioid system | 2008 | Rodent behavioural pharmacology with genetic and pharmacological kappa manipulation | Preclinical only | PMID DOI |
| Dynorphin A | A randomized proof-of-mechanism trial applying the 'fast-fail' approach to evaluating kappa-opioid antagonism as a treatment for anhedonia | 2020 | Multicentre 8-week double-blind placebo-controlled randomised trial in patients with anhedonia and a mood or anxiety disorder; selective kappa antagonist JNJ-67953964 10 mg (n=45) versus placebo (n=44) | PMID DOI | |
| Dynorphin A | Navacaprant in major depressive disorder (KOASTAL programme) | 2025 | Phase 3 randomised placebo-controlled trials | none | |
| Efinopegdutide | A phase IIa active-comparator-controlled study to evaluate the efficacy and safety of efinopegdutide in patients with non-alcoholic fatty liver disease | 2023 | 24-week randomised, active-comparator phase 2a trial, 145 adults with at least 10% liver fat (efinopegdutide 10 mg weekly n=72 versus semaglutide 1 mg weekly n=73), MRI-PDFF endpoint | PMID DOI Trial | |
| Efinopegdutide | A Clinical Study of Efinopegdutide in Participants With Precirrhotic Nonalcoholic Steatohepatitis (NASH) (MK-6024-013) | 2023 | Randomised phase 2b trial in 381 adults with biopsy-confirmed precirrhotic steatohepatitis, with efinopegdutide, semaglutide and placebo arms and a paired-biopsy histological endpoint | Trial | |
| Efinopegdutide | A Clinical Study of Efinopegdutide in People With Compensated Cirrhosis Due to Steatohepatitis (MK-6024-017) | 2024 | Phase 2a trial in 80 adults with compensated cirrhosis (F4 fibrosis) due to steatohepatitis, efinopegdutide versus placebo | Trial | |
| Efinopegdutide | Efficacy and safety of glucagon-like peptide-1/glucagon receptor co-agonist JNJ-64565111 in individuals with obesity without type 2 diabetes mellitus: A randomized dose-ranging study | 2021 | 26-week randomised, double-blind, placebo-controlled and open-label liraglutide-controlled parallel-group multicentre phase 2 dose-ranging trial, 474 randomised, 343 (72.4%) completed | PMID | |
| Elabela | Elabela/Toddler Is an Endogenous Agonist of the Apelin APJ Receptor in the Adult Cardiovascular System, and Exogenous Administration of the Peptide Compensates for the Downregulation of Its Expression in Pulmonary Arterial Hypertension | 2017 | Human tissue expression, receptor pharmacology and in vivo animal administration | Preclinical only | PMID |
| Elabela | In vitro metabolism of synthetic Elabela/Toddler (ELA-32) peptide in human plasma and kidney homogenates analyzed with mass spectrometry and validation of endogenous peptide quantification in tissues by ELISA | 2021 | Mass spectrometry degradation study with ELISA validation | Preclinical only | PMID DOI |
| Elabela | International Union of Basic and Clinical Pharmacology. CVII. Structure and Pharmacology of the Apelin Receptor with a Recommendation that Elabela/Toddler Is a Second Endogenous Peptide Ligand of the Apelin Receptor | 2019 | IUPHAR expert receptor nomenclature and pharmacology review | PMID DOI | |
| Elamipretide | Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy: The MMPOWER-3 Randomized Clinical Trial | 2023 | Randomised double-blind placebo-controlled phase 3, n=218 (109 elamipretide, 109 placebo), 24 weeks, 40 mg/day subcutaneous | High-quality evidence | PMID DOI Trial |
| Elamipretide | A phase 2/3 randomized clinical trial followed by an open-label extension to evaluate the effectiveness of elamipretide in Barth syndrome, a genetic disorder of mitochondrial cardiolipin metabolism | 2021 | Randomised double-blind placebo-controlled crossover, n=12, 40 mg/day for 12 weeks per arm with a 4-week washout, followed by an open-label extension in which 10 continued and 8 reached 36 weeks | Mixed evidence | PMID DOI Trial |
| Elamipretide | Long-term efficacy and safety of elamipretide in patients with Barth syndrome: 168-week open-label extension results of TAZPOWER | 2024 | Open-label extension, 168 weeks, no control group | Limited evidence | PMID DOI |
| Elamipretide | Randomized dose-escalation trial of elamipretide in adults with primary mitochondrial myopathy | 2018 | Randomised double-blind placebo-controlled phase 1/2 (MMPOWER), n=36, intravenous elamipretide at 0.01, 0.1 and 0.25 mg/kg/h infused over 2 hours in a dose-escalating sequence, six-minute walk measured after 5 days | Mixed evidence | PMID DOI |
| Elamipretide | Effects of Elamipretide on Left Ventricular Function in Patients With Heart Failure With Reduced Ejection Fraction: The PROGRESS-HF Phase 2 Trial | 2020 | Randomised double-blind placebo-controlled phase 2, 4 weeks | High-quality evidence | PMID DOI |
| Elamipretide | ReCLAIM-2: A Randomized Phase II Clinical Trial Evaluating Elamipretide in Age-related Macular Degeneration, Geographic Atrophy Growth, Visual Function, and Ellipsoid Zone Preservation | 2025 | Randomised placebo-controlled phase 2, n=176, dry AMD with non-central geographic atrophy | High-quality evidence | PMID DOI Trial |
| Elamipretide | The mitochondrial-targeted compound SS-31 re-energizes ischemic mitochondria by interacting with cardiolipin | 2013 | Mechanistic, isolated mitochondria and ischaemic kidney model | Preclinical only | PMID DOI |
| Elcatonin | Effect of elcatonin versus nonsteroidal anti-inflammatory medications for acute back pain in patients with osteoporotic vertebral fracture: a multiclinic randomized controlled trial | 2017 | Multicentre randomised controlled trial; 228 Japanese women with acute lumbar pain from osteoporotic vertebral fracture; weekly intramuscular elcatonin 20 units versus oral NSAIDs. Published as 35(4):375-384. | PMID DOI | |
| Elcatonin | Efficacy and safety of elcatonin in postmenopausal women with osteoporosis: a systematic review with network meta-analysis of randomized clinical trials | 2019 | Systematic review with network meta-analysis; 16 randomised trials, 2,754 postmenopausal women with osteoporosis. Published as 30(9):1723-1732. | PMID DOI | |
| Elcatonin | Anti-nociceptive effects of elcatonin injection for postmenopausal women with back pain: a randomized controlled trial | 2010 | Randomised controlled trial of elcatonin injection for back pain in postmenopausal women with osteoporosis. Published as 4:132-6. | PMID DOI | |
| Elcatonin | Ovariectomy-induced hyperalgesia and antinociceptive effect of elcatonin, a synthetic eel calcitonin | 1998 | Preclinical study in ovariectomised rats using nociceptive threshold testing. Published as 60(2):371-6. | PMID DOI | |
| Endothelin-1 | A novel potent vasoconstrictor peptide produced by vascular endothelial cells | 1988 | Peptide isolation, sequencing and cDNA cloning from porcine aortic endothelial cells | PMID | |
| Endothelin-1 | Bosentan therapy for pulmonary arterial hypertension | 2002 | Randomised double-blind placebo-controlled phase 3 trial (BREATHE-1) | PMID | |
| Endothelin-1 | Macitentan and morbidity and mortality in pulmonary arterial hypertension | 2013 | Long-term event-driven randomised double-blind placebo-controlled phase 3 trial (SERAPHIN) | PMID | |
| Endothelin-1 | Sparsentan in patients with IgA nephropathy: a prespecified interim analysis from a randomised, double-blind, active-controlled clinical trial | 2023 | Phase 3 randomised double-blind active-controlled trial versus irbesartan (PROTECT) | PMID | |
| Endothelin-1 | Efficacy and safety of sparsentan versus irbesartan in patients with IgA nephropathy (PROTECT): 2-year results from a randomised, active-controlled, phase 3 trial | 2023 | Two-year results of a phase 3 randomised active-controlled trial | PMID | |
| Endothelin-1 | Dual endothelin antagonist aprocitentan for resistant hypertension (PRECISION): a multicentre, blinded, randomised, parallel-group, phase 3 trial | 2022 | Phase 3 randomised blinded parallel-group trial with randomised withdrawal | PMID | |
| enfuvirtide | Enfuvirtide, an HIV-1 fusion inhibitor, for drug-resistant HIV infection in North and South America | 2003 | Randomised controlled open-label phase 3, 501 treatment-experienced patients randomised 2:1 to enfuvirtide plus optimised background regimen or the regimen alone | PMID | |
| enfuvirtide | Efficacy of enfuvirtide in patients infected with drug-resistant HIV-1 in Europe and Australia | 2003 | Randomised controlled open-label phase 3, 512 treatment-experienced patients, identical design to TORO 1 in a separate geography | PMID | |
| enfuvirtide | Durable efficacy of enfuvirtide over 48 weeks in heavily treatment-experienced HIV-1-infected patients in the T-20 versus optimized background regimen only 1 and 2 clinical trials | 2005 | Pre-specified pooled 48-week analysis of the TORO 1 and TORO 2 randomised trials | PMID | |
| Epitalon | Epithalon peptide induces telomerase activity and telomere elongation in human somatic cells | 2003 | In vitro, telomerase-negative human fetal fibroblast culture | Preclinical only | PMID DOI |
| Epitalon | Effect of Epitalon on biomarkers of aging, life span and spontaneous tumor incidence in female Swiss-derived SHR mice | 2003 | Rodent lifespan study, female outbred SHR mice, 54 per group, 1.0 microgram/mouse subcutaneously on 5 consecutive days monthly from 3 months of age until natural death | Preclinical only | PMID DOI |
| Epitalon | Inhibitory effect of the peptide epitalon on the development of spontaneous mammary tumors in HER-2/neu transgenic mice | 2002 | Transgenic mouse carcinogenesis model, female FVB/N HER-2/neu mice, 1 microgram/mouse subcutaneously for 5 consecutive days monthly from 2 months of age | Preclinical only | PMID DOI |
| Epitalon | Peptides of pineal gland and thymus prolong human life | 2003 | Non-randomised open clinical follow-up, 266 elderly subjects, 6-8 years of observation with treatment given in the first 2-3 years | Limited evidence | PMID |
| Epitalon | AEDG Peptide (Epitalon) Stimulates Gene Expression and Protein Synthesis during Neurogenesis: Possible Epigenetic Mechanism | 2020 | In vitro, human gingival mesenchymal stem cells, plus in silico molecular modelling of histone binding | Preclinical only | PMID DOI |
| Epitalon | Penetration of short fluorescence-labeled peptides into the nucleus in HeLa cells and in vitro specific interaction of the peptides with deoxyribooligonucleotides and DNA | 2011 | In vitro, fluorescence microscopy in HeLa cells and oligonucleotide fluorescence-quenching binding assays | Preclinical only | PMID DOI |
| Epitalon | Overview of Epitalon - Highly Bioactive Pineal Tetrapeptide with Promising Properties | 2025 | Narrative review of roughly 25 years of literature | Preclinical only | PMID DOI |
| Eptifibatide | Randomised placebo-controlled trial of effect of eptifibatide on complications of percutaneous coronary intervention: IMPACT-II | 1997 | Randomised, double-blind, placebo-controlled trial; 4,010 patients at 82 US centres undergoing percutaneous coronary intervention (placebo n=1,328; eptifibatide 135/0.5 n=1,349; eptifibatide 135/0.75 n=1,333) | PMID DOI | |
| Eptifibatide | Inhibition of platelet glycoprotein IIb/IIIa with eptifibatide in patients with acute coronary syndromes | 1998 | Randomised, double-blind, placebo-controlled trial; 10,948 patients with acute coronary syndrome without persistent ST elevation, enrolled November 1995 to January 1997 | PMID DOI | |
| Eptifibatide | Novel dosing regimen of eptifibatide in planned coronary stent implantation (ESPRIT): a randomised, placebo-controlled trial | 2000 | Randomised, double-blind, placebo-controlled trial; 2,064 patients undergoing planned stent implantation in native coronary arteries, higher-dose double-bolus regimen | PMID DOI | |
| Eptifibatide | Early versus delayed, provisional eptifibatide in acute coronary syndromes | 2009 | Randomised, double-blind trial; 9,492 patients with high-risk non-ST-elevation acute coronary syndrome, routine early eptifibatide (≥12 hours before angiography) versus delayed provisional use after angiography | PMID DOI | |
| Etelcalcetide | Effect of etelcalcetide vs placebo on serum parathyroid hormone in patients receiving hemodialysis with secondary hyperparathyroidism: two randomized clinical trials | 2017 | Two identically designed randomised, double-blind, placebo-controlled phase 3 trials; just over 1,000 haemodialysis patients with moderate to severe secondary hyperparathyroidism; 26 weeks. Published as 317(2):146-155. | PMID DOI Trial | |
| Etelcalcetide | Effect of etelcalcetide vs cinacalcet on serum parathyroid hormone in patients receiving hemodialysis with secondary hyperparathyroidism: a randomized clinical trial | 2017 | Randomised, double-blind, double-dummy active-comparator trial; n=683 haemodialysis patients; intravenous etelcalcetide versus oral cinacalcet; 26 weeks. Published as 317(2):156-164. | PMID DOI Trial | |
| Etelcalcetide | Critical cysteine residues in both the calcium-sensing receptor and the allosteric activator AMG 416 underlie the mechanism of action | 2015 | In vitro pharmacology and site-directed mutagenesis of the calcium-sensing receptor. Published as 88(5):853-65. | PMID DOI | |
| Etelcalcetide | Effect of cinacalcet on cardiovascular disease in patients undergoing dialysis | 2012 | Randomised, double-blind, placebo-controlled event-driven trial; over 3,800 haemodialysis patients with secondary hyperparathyroidism; composite cardiovascular and mortality primary endpoint. Published as 367(26):2482-2494. | PMID DOI | |
| Exenatide | Effects of exenatide (exendin-4) on glycemic control and weight over 30 weeks in metformin-treated patients with type 2 diabetes | 2005 | 30-week randomised, triple-blind, placebo-controlled phase 3 trial (AMIGO programme) across 82 US sites, 336 metformin-treated adults randomised, 272 completed | PMID DOI | |
| Exenatide | Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes | 2004 | 30-week randomised, triple-blind, placebo-controlled phase 3 trial, 377 sulfonylurea-treated adults | PMID DOI | |
| Exenatide | Effects of exenatide (exendin-4) on glycemic control over 30 weeks in patients with type 2 diabetes treated with metformin and a sulfonylurea | 2005 | 30-week randomised, triple-blind, placebo-controlled phase 3 trial, 733 adults on dual oral therapy | PMID DOI | |
| Exenatide | Exenatide once weekly versus twice daily for the treatment of type 2 diabetes: a randomised, open-label, non-inferiority study | 2008 | 30-week randomised open-label non-inferiority trial, 295 adults | PMID DOI | |
| Exenatide | Effects of Once-Weekly Exenatide on Cardiovascular Outcomes in Type 2 Diabetes | 2017 | Randomised, double-blind, placebo-controlled cardiovascular outcomes trial, 14,752 participants, median follow-up 3.2 years | PMID DOI Trial | |
| Follistatin (FST) | Follistatin complexes Myostatin and antagonises Myostatin-mediated inhibition of myogenesis | 2004 | In vitro complex formation and chick embryo myogenesis assays | Preclinical only | PMID DOI |
| Follistatin (FST) | The structure of myostatin:follistatin 288: insights into receptor utilization and heparin binding | 2009 | X-ray crystallography of the myostatin:FS-288 complex | Preclinical only | PMID DOI |
| Follistatin (FST) | Biological activity of follistatin isoforms and follistatin-like-3 is dependent on differential cell surface binding and specificity for activin, myostatin, and bone morphogenetic proteins | 2006 | Comparative binding and bioactivity assays across follistatin isoforms and follistatin-like-3 | Preclinical only | PMID DOI |
| Follistatin (FST) | Follistatin gene delivery enhances muscle growth and strength in nonhuman primates | 2009 | AAV1-FS344 intramuscular gene delivery in non-human primates with longitudinal follow-up | Preclinical only | PMID DOI |
| Follistatin (FST) | A phase 1/2a follistatin gene therapy trial for becker muscular dystrophy | 2015 | Open-label, non-randomised, uncontrolled dose-escalation; n=6; bilateral intramuscular AAV1.CMV.FS344 at 3 x 10^11 or 6 x 10^11 vg/kg per leg | Limited evidence | PMID DOI Trial |
| Follistatin (FST) | Follistatin Gene Therapy for Sporadic Inclusion Body Myositis Improves Functional Outcomes | 2017 | Open-label; n=6 treated with rAAV1.CMV.huFS344 at 6 x 10^11 vg/kg by bilateral quadriceps injection, compared with 8 untreated subjects | Limited evidence | PMID DOI Trial |
| FOXO4-DRI | Targeted Apoptosis of Senescent Cells Restores Tissue Homeostasis in Response to Chemotoxicity and Aging | 2017 | In vitro senescent cell assays plus in vivo work in Xpd progeroid, doxorubicin-treated and naturally aged mice | Preclinical only | PMID DOI |
| FOXO4-DRI | The disordered p53 transactivation domain is the target of FOXO4 and the senolytic compound FOXO4-DRI | 2025 | Solution NMR structural models and biophysical characterisation of the FOXO4-p53 and FOXO4-DRI-p53 complexes | Preclinical only | PMID DOI |
| FOXO4-DRI | FOXO4-DRI alleviates age-related testosterone secretion insufficiency by targeting senescent Leydig cells in aged mice | 2020 | Aged mouse model, Leydig cell senescence | Preclinical only | PMID DOI |
| FOXO4-DRI | Eliminating Senescent Cells Can Promote Pulmonary Hypertension Development and Progression | 2023 | Mouse and rat pulmonary hypertension models with senescent cell clearance by three independent methods: a p16 promoter-driven suicide gene, ABT263, and FOXO4-DRI; plus lung tissue from patients with pulmonary arterial hypertension | Preclinical only | PMID DOI |
| Galanin | Galanin - a novel biologically active peptide from porcine intestine | 1983 | Peptide isolation and sequencing | PMID | |
| Galanin | Developing novel antiepileptic drugs: characterization of NAX 5055, a systemically-active galanin analog, in epilepsy models | 2009 | Preclinical pharmacology across three rodent seizure models | Preclinical only | PMID |
| Galanin | Galanin receptors: IUPHAR/BPS Guide to Pharmacology classification | 2023 | Expert receptor nomenclature and pharmacology resource | none | |
| gallium (68Ga) dotatate | Prospective study of 68Ga-DOTATATE positron emission tomography/computed tomography for detecting gastro-entero-pancreatic neuroendocrine tumors and unknown primary sites | 2016 | Prospective single-institution diagnostic accuracy study, 131 patients, compared with 111In-pentetreotide SPECT/CT and anatomical imaging | PMID DOI | |
| gallium (68Ga) dotatate | 68Ga-DOTATATE compared with 111In-DTPA-octreotide and conventional imaging for pulmonary and gastroenteropancreatic neuroendocrine tumors: a systematic review and meta-analysis | 2016 | Systematic review and meta-analysis of diagnostic accuracy studies; 2,479 records screened, 42 articles included | PMID DOI | |
| gallium (68Ga) dotatate | Safety and efficacy of 68Ga-DOTATATE PET/CT for diagnosis, staging, and treatment management of neuroendocrine tumors | 2016 | Prospective study of diagnostic performance and management impact; 97 consecutively enrolled patients, of whom 78 had both 68Ga-DOTATATE PET/CT and 111In-pentetreotide imaging | PMID DOI | |
| gallium (68Ga) gozetotide | Assessment of 68Ga-PSMA-11 PET accuracy in localizing recurrent prostate cancer: a prospective single-arm clinical trial | 2019 | Prospective single-arm multicentre diagnostic accuracy trial, 635 men with biochemically recurrent prostate cancer | PMID DOI | |
| gallium (68Ga) gozetotide | Prostate-specific membrane antigen PET-CT in patients with high-risk prostate cancer before curative-intent surgery or radiotherapy (proPSMA): a prospective, randomised, multicentre study | 2020 | Prospective randomised multicentre comparison of PSMA PET/CT against conventional CT plus bone scintigraphy, 302 men with high-risk disease | PMID DOI | |
| gallium (68Ga) gozetotide | Diagnostic accuracy of 68Ga-PSMA-11 PET for pelvic nodal metastasis detection prior to radical prostatectomy and pelvic lymph node dissection: a multicenter prospective phase 3 imaging trial | 2021 | Multicentre prospective single-arm phase 3 diagnostic efficacy trial; 764 men enrolled and imaged, of whom 277 (36%) underwent prostatectomy with pelvic lymph node dissection and formed the efficacy analysis cohort | PMID DOI | |
| Ganirelix | Treatment with the gonadotrophin-releasing hormone antagonist ganirelix in women undergoing ovarian stimulation with recombinant follicle stimulating hormone is effective, safe and convenient: results of a controlled, randomized, multicentre trial | 2000 | Multicentre randomised controlled non-inferiority trial, 730 women randomised 2:1, ganirelix versus intranasal buserelin long protocol with recombinant FSH | PMID | |
| Ganirelix | Gonadotrophin-releasing hormone antagonists for assisted reproductive technology | 2016 | Cochrane systematic review and meta-analysis of randomised trials of antagonist versus agonist long protocols | PMID DOI | |
| Ganirelix | Comparison of GnRH antagonist with long GnRH agonist protocol after OCP pretreatment in PCOs patients | 2010 | Randomised comparison of antagonist versus long agonist protocol in women with polycystic ovary syndrome | PMID | |
| Gastrin | The constitution and properties of two gastrins extracted from hog antral mucosa | 1964 | Peptide isolation and structural characterisation | PMID | |
| Gastrin | Netazepide, a gastrin receptor antagonist, normalises tumour biomarkers and causes regression of type 1 gastric neuroendocrine tumours in a nonrandomised trial of patients with chronic atrophic gastritis | 2013 | Two-centre, 12-week open-label nonrandomised trial, 16 patients | PMID DOI | |
| Gastrin | Netazepide, a gastrin/cholecystokinin-2 receptor antagonist, can eradicate gastric neuroendocrine tumours in patients with autoimmune chronic atrophic gastritis | 2017 | Long-term open-label treatment in patients with type 1 gastric neuroendocrine tumours | PMID | |
| Gastrin | Randomized controlled trial of the gastrin/CCK2 receptor antagonist netazepide in patients with Barrett's esophagus | 2021 | Randomised, placebo-controlled trial in patients with non-dysplastic Barrett's oesophagus | PMID | |
| Ghrelin | Ghrelin is a growth-hormone-releasing acylated peptide from stomach | 1999 | Reverse pharmacology, peptide isolation and characterisation | PMID | |
| Ghrelin | Ghrelin enhances appetite and increases food intake in humans | 2001 | Randomised, double-blind, placebo-controlled crossover infusion study in healthy volunteers | PMID | |
| Ghrelin | A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans | 2001 | Human observational study with frequent sampling around fixed meal times | PMID | |
| Ghrelin | Elevated circulating level of ghrelin in cachexia associated with chronic heart failure: relationships between ghrelin and anabolic/catabolic factors | 2001 | Human observational study in cachectic and non-cachectic heart failure patients | PMID | |
| Ghrelin | Ghrelin treatment of cachectic patients with chronic obstructive pulmonary disease: a multicenter, randomized, double-blind, placebo-controlled trial | 2012 | Multicentre randomised, double-blind, placebo-controlled trial, 33 cachectic COPD patients, intravenous ghrelin twice daily for 3 weeks | PMID DOI | |
| Ghrelin | Anamorelin in patients with non-small-cell lung cancer and cachexia (ROMANA 1 and ROMANA 2): results from two randomised, double-blind, phase 3 trials | 2016 | Two randomised, double-blind, placebo-controlled phase 3 trials of an oral GHSR agonist in cancer cachexia | PMID DOI | |
| GHRP-1 | Growth hormone-releasing activity of growth hormone-releasing peptide-1 (a synthetic heptapeptide) in children and adolescents | 1993 | Open-label single intravenous bolus growth hormone provocation study in 15 short but healthy children and adolescents (6 prepubertal, 9 pubertal) and 8 juvenile patients with pituitary insufficiency | PMID DOI | |
| GHRP-1 | Design, synthesis, and biological activity of peptides which release growth hormone in vitro | 1981 | Preclinical structure-activity study of enkephalin-derived peptides on rat pituitary cells, guided by conformational analysis | Preclinical only | PMID |
| GHRP-1 | Conformational energy studies and in vitro and in vivo activity data on growth hormone-releasing peptides | 1984 | Preclinical conformational energy modelling with in vitro and in vivo activity testing in rats | Preclinical only | PMID |
| GHRP-1 | Structure-activity relationship for peptidic growth hormone secretagogues | 2017 | Experimental structure-activity study using a radio-competitive GHS-R1a binding assay against radiolabelled ghrelin, with receptor-assay activity measured in samples from excretion studies after intranasal administration | Preclinical only | PMID DOI |
| GHRP-1 | Growth hormone-releasing peptides | 1997 | Narrative review of GHRP pharmacology in animals and humans | PMID DOI | |
| GHRP-2 (pralmorelin) | A simple diagnostic test using GH-releasing peptide-2 in adult GH deficiency | 2007 | International diagnostic validation study; 77 healthy subjects and 58 patients with peak GH below 3 micrograms/L on an insulin tolerance test; 100 micrograms intravenous GHRP-2 with sampling over 2 hours | Mixed evidence | PMID DOI |
| GHRP-2 (pralmorelin) | Effects of eight months treatment with graded doses of a growth hormone (GH)-releasing peptide in GH-deficient children | 1998 | Uncontrolled dose-escalation study, n=6 prepubertal children with growth hormone deficiency; subcutaneous GHRP-2 at 0.3, 1.0 and 3.0 micrograms/kg/day over successive 2-month periods across 8 months | Limited evidence | PMID DOI |
| GHRP-2 (pralmorelin) | Growth hormone releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men | 2005 | Crossover study, n=7 lean healthy men, GHRP-2 infusion versus saline followed by an ad libitum buffet meal | Limited evidence | PMID DOI |
| GHRP-2 (pralmorelin) | Pharmacokinetics and pharmacodynamics of growth hormone-releasing peptide-2: a phase I study in children | 1998 | Phase 1 pharmacokinetic study, n=10 prepubertal children (mean age 7.7 years), single 1 microgram/kg intravenous dose with sampling over 2 hours | Limited evidence | PMID DOI |
| GHRP-2 (pralmorelin) | Growth hormone (GH)-releasing peptide stimulates GH release in normal men and acts synergistically with GH-releasing hormone | 1990 | Dose-ranging intravenous study in normal men, GHRP alone and combined with GHRH | Mixed evidence | PMID DOI |
| GHRP-4 | In-house standards derived from doping peptides: Enzymatic and serum stability and degradation profile of GHRP and GHRH-related peptides | 2023 | Solid-phase synthesis of six GHRP and GHRH-related peptides with in vitro enzymatic and human serum stability and degradation profiling | PMID DOI | |
| GHRP-4 | Determination of growth hormone releasing peptides (GHRP) and their major metabolites in human urine for doping controls by means of liquid chromatography mass spectrometry | 2011 | Analytical method development and validation for GHRP detection in human urine, with a proof-of-concept administration study | PMID DOI | |
| GHRP-4 | Design, synthesis, and biological activity of peptides which release growth hormone in vitro | 1981 | Preclinical structure-activity screen of enkephalin-derived peptides on rat pituitary cells | Preclinical only | PMID |
| GHRP-4 | Conformational energy studies and in vitro and in vivo activity data on growth hormone-releasing peptides | 1984 | Preclinical conformational energy modelling with in vitro and in vivo rat activity data | Preclinical only | PMID |
| GHRP-4 | Structure-activity relationship for peptidic growth hormone secretagogues | 2017 | Radio-competitive GHS-R1a binding assay against radiolabelled ghrelin, with receptor-assay activity measured in excretion-study urine after intranasal dosing | Preclinical only | PMID DOI |
| GHRP-5 | Prolactin-releasing activity of GHRP-5 (Momany peptide) on lactotrophs in vivo and in vitro | 2002 | Rat in vivo treatment plus in vitro pituitary and enriched lactotroph cell culture | Preclinical only | PMID |
| GHRP-5 | Design, synthesis, and biological activity of peptides which release growth hormone in vitro | 1981 | Preclinical structure-activity screen of enkephalin-derived peptides on rat pituitary cells | Preclinical only | PMID |
| GHRP-5 | Conformational energy studies and in vitro and in vivo activity data on growth hormone-releasing peptides | 1984 | Preclinical conformational energy modelling with rat in vitro and in vivo activity data | Preclinical only | PMID |
| GHRP-5 | Adsorption effects of the doping relevant peptides Insulin Lispro, Synachten, TB-500 and GHRP 5 | 2017 | Analytical study of peptide adsorption to consumable surfaces during sample preparation | PMID DOI | |
| GHRP-6 | On the in vitro and in vivo activity of a new synthetic hexapeptide that acts on the pituitary to specifically release growth hormone | 1984 | In vitro pituitary cell and in vivo studies across rats, monkeys, lambs, calves and chicks | Preclinical only | PMID DOI |
| GHRP-6 | Growth hormone (GH)-releasing peptide stimulates GH release in normal men and acts synergistically with GH-releasing hormone | 1990 | Dose-ranging intravenous study in normal men, GHRP-6 alone and combined with GHRH | Mixed evidence | PMID DOI |
| GHRP-6 | Growth hormone (GH)-releasing peptide-6 requires endogenous hypothalamic GH-releasing hormone for maximal GH stimulation | 1998 | Human endocrine challenge study | Mixed evidence | PMID DOI |
| GHRP-6 | Growth-hormone-releasing peptide 6 (GHRP6) prevents oxidant cytotoxicity and reduces myocardial necrosis in a model of acute myocardial infarction | 2007 | Cell culture and animal model of acute myocardial infarction | Preclinical only | PMID DOI |
| GHRP-6 | A receptor in pituitary and hypothalamus that functions in growth hormone release | 1996 | Molecular cloning and characterisation of the growth hormone secretagogue receptor from swine and human pituitary and hypothalamus | Preclinical only | PMID DOI |
| Glucagon | Intranasal Glucagon for Treatment of Insulin-Induced Hypoglycemia in Adults With Type 1 Diabetes: A Randomized Crossover Noninferiority Study | 2016 | Randomised crossover non-inferiority study across eight clinical centres, 75 adults with type 1 diabetes (mean age 33, median duration 18 years), nasal glucagon 3 mg versus intramuscular glucagon 1 mg during insulin-induced hypoglycaemia | PMID DOI | |
| Glucagon | Glucagon Administration by Nasal and Intramuscular Routes in Adults With Type 1 Diabetes During Insulin-Induced Hypoglycaemia: A Randomised, Open-Label, Crossover Study | 2020 | Randomised, open-label, two-period crossover study at two sites, 66 adults with type 1 diabetes in the primary efficacy analysis | PMID DOI | |
| Glucagon | Nasal glucagon as a viable alternative for treating insulin-induced hypoglycaemia in Japanese patients with type 1 or type 2 diabetes: A phase 3 randomized crossover study | 2020 | Phase 3 randomised crossover study in Japanese adults with type 1 or type 2 diabetes | PMID DOI | |
| Glucagon | Effects of common cold and concomitant administration of nasal decongestant on the pharmacokinetics and pharmacodynamics of nasal glucagon in otherwise healthy participants: A randomized clinical trial | 2018 | Randomised clinical trial of nasal glucagon pharmacokinetics and pharmacodynamics during common cold, with and without decongestant | PMID DOI | |
| Glucagon-like peptide-1 (native) | Glucagon-like peptide-1 7-36: a physiological incretin in man | 1987 | Human infusion study with physiological and postprandial concentration matching | PMID DOI | |
| Glucagon-like peptide-1 (native) | Normalization of fasting hyperglycaemia by exogenous glucagon-like peptide 1 (7-36 amide) in type 2 (non-insulin-dependent) diabetic patients | 1993 | Controlled human infusion study in poorly controlled type 2 diabetic patients | PMID DOI | |
| Glucagon-like peptide-1 (native) | Preserved incretin activity of glucagon-like peptide 1 [7-36 amide] but not of synthetic human gastric inhibitory polypeptide in patients with type-2 diabetes mellitus | 1993 | Controlled human infusion study, 9 patients with type 2 diabetes and 9 matched controls | PMID DOI | |
| Glucagon-like peptide-1 (native) | Effect of 6-week course of glucagon-like peptide 1 on glycaemic control, insulin sensitivity, and beta-cell function in type 2 diabetes: a parallel-group study | 2002 | Parallel-group pilot study, 20 patients with type 2 diabetes (10 continuous subcutaneous GLP-1, 10 saline, one control excluded), 6 weeks | PMID | |
| Glucagon-like peptide-2 (native) | Induction of intestinal epithelial proliferation by glucagon-like peptide 2 | 1996 | Preclinical mouse study | PMID DOI | |
| Glucagon-like peptide-2 (native) | Glucagon-like peptide 2 improves nutrient absorption and nutritional status in short-bowel patients with no colon | 2001 | Open-label, uncontrolled study with formal balance studies, 8 patients, 35 days of native GLP-2 400 micrograms twice daily | PMID DOI | |
| Glucagon-like peptide-2 (native) | Glepaglutide, a novel long-acting glucagon-like peptide-2 analogue, for patients with short bowel syndrome: a randomised phase 2 trial | 2019 | Randomised, double-blind, dose-ranging phase 2 trial | PMID | |
| Glucagon-like peptide-2 (native) | Glepaglutide, a long-acting glucagon-like peptide-2 analogue, reduces parenteral support in patients with short bowel syndrome: a phase 3 randomized controlled trial | 2025 | International phase 3 randomised, placebo-controlled trial | PMID | |
| Glucose-dependent insulinotropic polypeptide (GIP) | Preserved incretin activity of glucagon-like peptide 1 [7-36 amide] but not of synthetic human gastric inhibitory polypeptide in patients with type-2 diabetes mellitus | 1993 | Controlled human infusion study, 9 patients with type 2 diabetes and 9 age- and weight-matched controls | PMID DOI | |
| Glucose-dependent insulinotropic polypeptide (GIP) | Stimulation of insulin secretion by gastric inhibitory polypeptide in man | 1973 | Human infusion study | PMID DOI | |
| Glucose-dependent insulinotropic polypeptide (GIP) | Four weeks of near-normalisation of blood glucose improves the insulin response to glucagon-like peptide-1 and glucose-dependent insulinotropic polypeptide in patients with type 2 diabetes | 2009 | Interventional human study with hyperglycaemic clamp and incretin infusions before and after glycaemic normalisation | PMID | |
| Glucose-dependent insulinotropic polypeptide (GIP) | Glucose-dependent insulinotropic polypeptide: a bifunctional glucose-dependent regulator of glucagon and insulin secretion in humans | 2011 | Human clamp study across a range of glucose concentrations with GIP infusion | PMID | |
| glycyl-L-histidyl-L-lysine | The interaction of copper(II) and glycyl-L-histidyl-L-lysine, a growth-modulating tripeptide from plasma | 1981 | Equilibrium and spectroscopic characterisation | PMID | |
| glycyl-L-histidyl-L-lysine | Structure of the Glycyl-L-histidyl-L-lysine--copper(II) complex in solution | 1982 | EPR, ENDOR and spectroscopic structural determination | PMID DOI | |
| glycyl-L-histidyl-L-lysine | Stimulation of sulfated glycosaminoglycan synthesis by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+ | 1992 | In vitro, cultured fibroblasts | Preclinical only | PMID DOI |
| glycyl-L-histidyl-L-lysine | The tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+ stimulates matrix metalloproteinase-2 expression by fibroblast cultures | 2000 | In vitro, human dermal fibroblasts | Preclinical only | PMID |
| glycyl-L-histidyl-L-lysine | Effect of Gly-Gly-His, Gly-His-Lys and their copper complexes on TNF-alpha-dependent IL-6 secretion in normal human dermal fibroblasts | 2012 | In vitro, normal human dermal fibroblasts | Preclinical only | PMID |
| glycyl-L-histidyl-L-lysine | Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data | 2018 | Narrative review | PMID | |
| glycyl-L-histidyl-L-lysine | D-tyrosine adds an anti-melanogenic effect to cosmetic peptides | 2020 | In vitro, MNT-1 melanoma cells, primary human melanocytes and a 3D human skin model | Preclinical only | PMID DOI |
| Gonadorelin | The Pulsatile Gonadorelin Pump Induces Earlier Spermatogenesis Than Cyclical Gonadotropin Therapy in Congenital Hypogonadotropic Hypogonadism Men | 2019 | Non-randomised comparative study over 24 months, n=28 azoospermic men (10 pulsatile gonadorelin pump, 18 cyclical hCG/hMG) | Limited evidence | PMID DOI |
| Gonadorelin | Efficacy and safety of pulsatile gonadotropin-releasing hormone therapy in patients with congenital hypogonadotropic hypogonadism: a multicentre clinical study | 2021 | Prospective, self-controlled clinical study over seven days, n=28 men with congenital hypogonadotropic hypogonadism, evaluating a pulsatile GnRH pump device | Limited evidence | PMID DOI |
| Gonadorelin | Hormonal control of spermatogenesis in men: therapeutic aspects in hypogonadotropic hypogonadism | 2014 | Narrative review of gonadotrophin and pulsatile GnRH therapy for fertility induction - not primary data | Limited evidence | PMID DOI |
| Gonadorelin | Genetic Profiles and Three-year Follow-up Study of Chinese Males With Congenital Hypogonadotropic Hypogonadism | 2021 | Three-year longitudinal cohort with whole-exome sequencing and quarterly clinical assessment, n=73 Chinese men with congenital hypogonadotropic hypogonadism | Limited evidence | PMID DOI |
| Goserelin | Improved survival in patients with locally advanced prostate cancer treated with radiotherapy and goserelin | 1997 | Randomised controlled trial (EORTC 22863), 415 men with locally advanced prostate cancer | PMID | |
| Goserelin | Long-term results with immediate androgen suppression and external irradiation in patients with locally advanced prostate cancer (an EORTC study): a phase III randomised trial | 2002 | Extended follow-up of EORTC 22863 randomised trial | PMID | |
| Goserelin | External irradiation with or without long-term androgen suppression for prostate cancer with high metastatic risk: 10-year results of an EORTC randomised study | 2010 | Ten-year follow-up of EORTC 22863 randomised trial | PMID | |
| Goserelin | Goserelin for ovarian protection during breast-cancer adjuvant chemotherapy | 2015 | Randomised controlled trial (POEMS/S0230), 257 premenopausal women with hormone receptor-negative breast cancer | PMID | |
| Gramicidin | Studies on a bactericidal agent extracted from a soil bacillus: I. Preparation of the agent. Its activity in vitro | 1939 | Foundational in vitro study of a bacterial culture extract (J Exp Med 70(1):1-10) | PMID DOI | |
| Gramicidin | Fractionation of the bactericidal agent from cultures of a soil bacillus | 1940 | Chemical fractionation study (J Biol Chem 132:791-792) | DOI | |
| Gramicidin | High-resolution conformation of gramicidin A in a lipid bilayer by solid-state NMR | 1993 | Structural biology study in oriented lipid bilayers (Science 261(5127):1457-60) | PMID DOI | |
| HEP-1 (Human Ezrin Peptide One) | Ezrin Peptide Therapy from HIV to COVID: Inhibition of Inflammation and Amplification of Adaptive Anti-Viral Immunity | 2021 | Narrative review by the peptide's developers, summarising uncontrolled clinical series and laboratory work; volume 22, article 11688 | Limited evidence | PMID DOI |
| HEP-1 (Human Ezrin Peptide One) | Administration of the immunomodulator gepon after tonsillectomy | 2005 | Russian-language clinical and immunological assessment in 37 patients with chronic tonsillitis before and after bilateral tonsillectomy; issue 3, pages 57-61 | Limited evidence | PMID |
| HEP-1 (Human Ezrin Peptide One) | The antiviral activity of peptide immunomodulator 'Gepon' in experimental infections caused by herpes simplex viruses types 1 and 2 | 2003 | Laboratory and in vivo experimental study of antiviral activity against HSV-1 and HSV-2; volume 48(5):30-33 | Preclinical only | PMID |
| HEP-1 (Human Ezrin Peptide One) | Local immune and oxidative status in exacerbated chronic apical periodontitis | 2017 | Russian-language study of salivary immune and oxidative markers in 67 patients (mean age 31±2.5 years) with exacerbated chronic apical periodontitis, before and after intervention; volume 96(3):26-29 | Limited evidence | PMID |
| HEP-1 (Human Ezrin Peptide One) | The Clinical Trial of Application of Ezrin Peptide (HEP-1) for Treatment of Coronavirus Disease (COVID-19) Infection | 2020 | Registered phase 1 study, 20 participants, COVID-19; sponsor Shahid Beheshti University of Medical Sciences | Limited evidence | Trial |
| hexapeptide-11 | Hexapeptide-11 is a novel modulator of the proteostasis network in human diploid fibroblasts | 2015 | In vitro, normal human diploid lung and skin fibroblasts, plus in vivo human skin deformation assays reported as a sub-experiment | Preclinical only | PMID DOI |
| hexapeptide-11 | Modulation of cellular senescence in fibroblasts and dermal papillae cells in vitro | 2013 | In vitro, intrinsically and extrinsically aged fibroblasts and dermal papilla cells | Preclinical only | PMID |
| hexapeptide-11 | Protective and Anti-Aging Effects of 5 Cosmeceutical Peptide Mixtures on Hydrogen Peroxide-Induced Premature Senescence in Human Skin Fibroblasts | 2021 | In vitro screen of five peptides individually for optimal concentration, then six mixtures | Preclinical only | PMID DOI |
| hexapeptide-11 | Identification of bioaccessible and neuroprotective peptides from fermented casein hydrolysate | 2025 | Peptidomic screen and microglial cell culture | Preclinical only | PMID DOI |
| Hexarelin | Growth hormone-releasing activity of hexarelin in humans. A dose-response study | 1994 | Double-blind, placebo-controlled rising-dose study, n=12 adult male volunteers, single intravenous boluses of 0.5, 1 and 2 micrograms/kg | Limited evidence | PMID DOI |
| Hexarelin | Growth hormone status during long-term hexarelin therapy | 1998 | 16-week study of hexarelin 1.5 micrograms/kg subcutaneously twice daily, with follow-up to 20 weeks; the abstract does not state the number of subjects | Limited evidence | PMID DOI |
| Hexarelin | Cardiac effects of hexarelin in hypopituitary adults | 1999 | Equilibrium radionuclide angiocardiography in 7 men with growth hormone deficiency and 9 controls after intravenous hexarelin | Limited evidence | PMID DOI |
| Hexarelin | CD36 mediates the cardiovascular action of growth hormone-releasing peptides in the heart | 2002 | Receptor purification and perfused heart studies including CD36-null mice and CD36-deficient spontaneously hypertensive rats | Preclinical only | PMID DOI |
| Hexarelin | Acute cardiovascular and hormonal effects of GH and hexarelin, a synthetic GH-releasing peptide, in humans | 1999 | Comparative radionuclide angiocardiography study of intravenous recombinant human growth hormone versus hexarelin in 7 male volunteers | Limited evidence | PMID DOI |
| HGH fragment 176-191 | Hyperglycemic action of synthetic C-terminal fragments of human growth hormone | 1978 | Preclinical; synthetic C-terminal fragments in animal models | Preclinical only | PMID DOI |
| HGH fragment 176-191 | Antilipogenic action of synthetic C-terminal sequence 177-191 of human growth hormone | 1993 | Preclinical; in vitro and rodent adipose tissue | Preclinical only | PMID |
| HGH fragment 176-191 | Effect of an antilipogenic fragment of human growth hormone on glucose transport in rat adipocytes | 1993 | Preclinical; isolated rat adipocytes | Preclinical only | PMID |
| HGH fragment 176-191 | Increase of fat oxidation and weight loss in obese mice caused by chronic treatment with human growth hormone or a modified C-terminal fragment | 2001 | Preclinical; chronic dosing in obese mice | Preclinical only | PMID DOI |
| HGH fragment 176-191 | The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta(3)-AR knock-out mice | 2001 | Preclinical; obese mice and beta-3 adrenergic receptor knockout mice | Preclinical only | PMID DOI |
| Histrelin | Efficacy and safety of histrelin subdermal implant in children with central precocious puberty: a multicenter trial | 2007 | Prospective single-arm open-label multicentre trial, 36 children with central precocious puberty, single 12-month subdermal implant. No control group. | PMID | |
| Histrelin | A single histrelin implant is effective for 2 years for treatment of central precocious puberty | 2013 | Observational cohort of children with central precocious puberty retaining a single implant beyond its nominal 12-month life | PMID | |
| human epidermal growth factor | Topical epidermal growth factor spray for the treatment of chronic diabetic foot ulcers: A phase III multicenter, double-blind, randomized, placebo-controlled trial | 2018 | Phase III multicentre double-blind randomised placebo-controlled trial, 167 patients at six centres (82 rhEGF, 85 saline), up to 12 weeks | PMID DOI | |
| human epidermal growth factor | Growth factors for treating diabetic foot ulcers | 2015 | Cochrane systematic review and meta-analysis of trials of 11 different growth factors | PMID DOI | |
| human epidermal growth factor | Efficacy and safety of recombinant human epidermal growth factor for diabetic foot ulcers: A systematic review and meta-analysis of randomised controlled trials | 2020 | Systematic review and meta-analysis of randomised controlled trials | PMID DOI | |
| human epidermal growth factor | The Effect of Micro-Spicule Containing Epidermal Growth Factor on Periocular Wrinkles | 2017 | Randomised controlled split-face study, 20 healthy volunteers aged 33 to 54, 4 weeks daily treatment with 8-week follow-up | PMID DOI | |
| human epidermal growth factor | Anti-Wrinkle Efficacy of Cross-Linked Hyaluronic Acid-Based Microneedle Patch with Acetyl Hexapeptide-8 and Epidermal Growth Factor on Korean Skin | 2019 | Clinical evaluation of a combination microneedle patch | PMID | |
| human epidermal growth factor | Retinoid-induced epidermal hyperplasia is mediated by epidermal growth factor receptor activation via specific induction of its ligands heparin-binding EGF and amphiregulin in human skin in vivo | 2006 | Human skin in vivo and cell culture | PMID | |
| Humanin | A rescue factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Abeta | 2001 | Expression cloning from human occipital lobe cDNA library, neuronal cell death assays | Preclinical only | PMID DOI |
| Humanin | Humanin: a novel central regulator of peripheral insulin action | 2009 | Rodent, intracerebroventricular and peripheral administration with hyperinsulinaemic-euglycaemic clamp | Preclinical only | PMID DOI |
| Humanin | Central effects of humanin on hepatic triglyceride secretion | 2015 | Rodent, central administration | Preclinical only | PMID DOI |
| Humanin | A humanin analog decreases oxidative stress and preserves mitochondrial integrity in cardiac myoblasts | 2013 | In vitro, cardiac myoblasts under oxidative stress | Preclinical only | PMID DOI |
| Humanin | Humanin Isoforms in Cardiac Muscle and Blood Plasma and Major Complications After Cardiac Operation | 2018 | Observational biomarker study, n=106, patients undergoing cardiac surgery; completed | Limited evidence | Trial |
| Icatibant | Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema | 2010 | Two parallel phase 3 randomised, double-blind, controlled trials in acute hereditary angioedema attacks, 130 patients in total: FAST-1 (56 patients) versus placebo, FAST-2 (74 patients) versus tranexamic acid | PMID DOI | |
| Icatibant | Randomized placebo-controlled trial of the bradykinin B2 receptor antagonist icatibant for the treatment of acute attacks of hereditary angioedema: the FAST-3 trial | 2011 | Phase 3, randomised, double-blind, placebo-controlled trial; 88 patients with moderate to very severe cutaneous or abdominal attacks (icatibant n=43, placebo n=45), plus a cohort of 10 subjects with laryngeal attacks | PMID DOI | |
| Icatibant | Randomized trial of icatibant for angiotensin-converting enzyme inhibitor-induced upper airway angioedema | 2017 | Randomised, double-blind, placebo-controlled trial; 121 patients randomised (icatibant 61, placebo 60; 118 treated) with at least moderately severe ACE-inhibitor-induced upper airway angioedema | PMID DOI | |
| Insulin aspart | Insulin aspart vs. human insulin in the management of long-term blood glucose control in Type 1 diabetes mellitus: a randomized controlled trial | 2000 | Six-month multicentre randomised open-label parallel-group trial, n=1,070 adults with type 1 diabetes | PMID | |
| Insulin aspart | Hypoglycaemia with insulin aspart: a double-blind, randomised, crossover trial in subjects with Type 1 diabetes | 2004 | Double-blind randomised crossover trial in adults with type 1 diabetes, aspart immediately before meals versus soluble human insulin | PMID | |
| Insulin aspart | Maternal glycemic control and hypoglycemia in type 1 diabetic pregnancy: a randomized trial of insulin aspart versus human insulin in 322 pregnant women | 2007 | Randomised controlled trial in 322 pregnant women with type 1 diabetes, insulin aspart versus regular human insulin as prandial insulin within a basal-bolus regimen with isophane insulin | PMID | |
| Insulin aspart | Short-acting insulin analogues versus regular human insulin for adults with type 1 diabetes mellitus | 2016 | Systematic review and meta-analysis of randomised controlled trials of rapid-acting analogues including aspart | PMID DOI | |
| Insulin aspart | Efficacy and Safety of Rapid-Acting Insulin Analogs in Special Populations with Type 1 Diabetes or Gestational Diabetes: Systematic Review and Meta-Analysis | 2018 | Systematic review and meta-analysis covering pregnancy, children and adolescents, and continuous subcutaneous insulin infusion | PMID | |
| Insulin degludec | Insulin degludec, an ultra-longacting basal insulin, versus insulin glargine in basal-bolus treatment with mealtime insulin aspart in type 1 diabetes (BEGIN Basal-Bolus Type 1): a phase 3, randomised, open-label, treat-to-target non-inferiority trial | 2012 | 52-week randomised open-label treat-to-target non-inferiority trial, n=629, type 1 diabetes | PMID DOI | |
| Insulin degludec | Insulin degludec versus insulin glargine in insulin-naive patients with type 2 diabetes: a 1-year, randomized, treat-to-target trial (BEGIN Once Long) | 2012 | 52-week randomised open-label treat-to-target non-inferiority trial, n=1,030, insulin-naive type 2 diabetes | PMID | |
| Insulin degludec | Efficacy and Safety of Degludec versus Glargine in Type 2 Diabetes | 2017 | Double-blind, treat-to-target, event-driven cardiovascular outcome trial, n=7,637 adults with type 2 diabetes at high cardiovascular risk, median follow-up about 2 years | PMID DOI | |
| Insulin degludec | Effect of Insulin Degludec vs Insulin Glargine U100 on Hypoglycemia in Patients With Type 1 Diabetes: The SWITCH 1 Randomized Clinical Trial | 2017 | Double-blind, randomised, two-period crossover treat-to-target trial, n=501 adults with type 1 diabetes and at least one hypoglycaemia risk factor | PMID | |
| Insulin degludec | Effect of Insulin Degludec vs Insulin Glargine U100 on Hypoglycemia in Patients With Type 2 Diabetes: The SWITCH 2 Randomized Clinical Trial | 2017 | Double-blind, randomised, two-period crossover treat-to-target trial, n=721 adults with type 2 diabetes and at least one hypoglycaemia risk factor | PMID | |
| Insulin detemir | Insulin detemir offers improved glycemic control compared with NPH insulin in people with type 1 diabetes: a randomized clinical trial | 2004 | Multicentre randomised open-label parallel-group trial, n=408 adults with type 1 diabetes, two twice-daily detemir regimens versus isophane insulin | PMID | |
| Insulin detemir | A 26-week, randomized, parallel, treat-to-target trial comparing insulin detemir with NPH insulin as add-on therapy to oral glucose-lowering drugs in insulin-naive people with type 2 diabetes | 2006 | 26-week randomised open-label parallel-group treat-to-target trial, n=476, insulin-naive type 2 diabetes on oral agents | PMID | |
| Insulin detemir | A randomised, 52-week, treat-to-target trial comparing insulin detemir with insulin glargine when administered as add-on to glucose-lowering drugs in insulin-naive people with type 2 diabetes | 2008 | 52-week multinational randomised open-label parallel-group non-inferiority trial, n=582, insulin-naive type 2 diabetes | PMID DOI | |
| Insulin detemir | Addition of biphasic, prandial, or basal insulin to oral therapy in type 2 diabetes | 2007 | Three-arm randomised open-label trial, n=708 adults with type 2 diabetes inadequately controlled on metformin and a sulfonylurea, one-year report | PMID DOI | |
| Insulin detemir | Three-year efficacy of complex insulin regimens in type 2 diabetes | 2009 | Three-year extension of the 4-T trial with protocol-driven intensification, n=708 | PMID DOI | |
| Insulin glargine | The treat-to-target trial: randomized addition of glargine or human NPH insulin to oral therapy of type 2 diabetic patients | 2003 | 24-week randomised, open-label, parallel-group treat-to-target trial, n=756 adults with type 2 diabetes inadequately controlled on oral agents | PMID DOI | |
| Insulin glargine | Less hypoglycemia with insulin glargine in intensive insulin therapy for type 1 diabetes | 2000 | Pooled analysis of two 28-week multicentre randomised open-label trials in adults with type 1 diabetes on multiple daily injections | PMID DOI | |
| Insulin glargine | Basal insulin and cardiovascular and other outcomes in dysglycemia | 2012 | Randomised 2x2 factorial cardiovascular outcome trial, n=12,537, median follow-up 6.2 years, glargine titrated to fasting glucose ≤5.3 mmol/L versus standard care | PMID DOI | |
| Insulin glargine | Long-acting insulin analogues versus NPH insulin (human isophane insulin) for type 2 diabetes mellitus | 2007 | Systematic review and meta-analysis of randomised controlled trials | PMID DOI | |
| Insulin glargine | Association of Initiation of Basal Insulin Analogs vs Neutral Protamine Hagedorn Insulin With Hypoglycemia-Related Emergency Department Visits or Hospital Admissions and With Glycemic Control in Patients With Type 2 Diabetes | 2018 | Retrospective observational cohort with propensity-score matching, n=25,489 adults with type 2 diabetes initiating basal insulin in routine care | PMID DOI | |
| Insulin glulisine | Insulin glulisine provides improved glycemic control in patients with type 2 diabetes | 2004 | 26-week multicentre randomised open-label parallel-group trial, n=876 adults with type 2 diabetes, glulisine or regular human insulin each combined with isophane insulin | PMID DOI | |
| Insulin glulisine | Optimized Basal-bolus insulin regimens in type 1 diabetes: insulin glulisine versus regular human insulin in combination with Basal insulin glargine | 2005 | 12-week randomised trial, n=860 adults with type 1 diabetes, three arms: premeal glulisine, postmeal glulisine, and premeal regular human insulin, all with basal glargine | PMID | |
| Insulin glulisine | Short-acting insulin analogues versus regular human insulin for adults with type 1 diabetes mellitus | 2016 | Systematic review and meta-analysis of randomised controlled trials of rapid-acting analogues including glulisine | PMID DOI | |
| Insulin glulisine | Efficacy and Safety of Rapid-Acting Insulin Analogs in Special Populations with Type 1 Diabetes or Gestational Diabetes: Systematic Review and Meta-Analysis | 2018 | Systematic review and meta-analysis covering pregnancy, children and adolescents, and continuous subcutaneous insulin infusion | PMID | |
| Insulin human (regular) | Human insulin produced by recombinant DNA technology: safety and hypoglycaemic potency in healthy men | 1980 | First-in-human comparative study of biosynthetic human insulin against purified animal insulin in healthy male volunteers | PMID | |
| Insulin human (regular) | The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus | 1993 | Randomised controlled trial of intensive versus conventional insulin therapy, 1,441 people with type 1 diabetes, mean follow-up 6.5 years | PMID DOI | |
| Insulin human (regular) | Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33) | 1998 | Randomised controlled trial of intensive versus conventional glycaemic control, 3,867 people with newly diagnosed type 2 diabetes, median follow-up 10 years | PMID DOI | |
| Insulin human (regular) | Reduction of postprandial hyperglycemia and frequency of hypoglycemia in IDDM patients on insulin-analog treatment | 1997 | Multicentre randomised crossover trial comparing insulin lispro with regular human insulin in insulin-dependent diabetes | PMID | |
| Insulin human (regular) | Intensive versus conventional glucose control in critically ill patients | 2009 | Randomised controlled trial of intensive intravenous insulin therapy versus conventional glucose targets, 6,104 intensive care unit patients | PMID DOI | |
| Insulin icodec | Weekly Icodec versus Daily Glargine U100 in Type 2 Diabetes without Previous Insulin | 2023 | 78-week phase 3a randomised open-label treat-to-target trial, n=984 insulin-naive adults with type 2 diabetes | PMID DOI | |
| Insulin icodec | Once-Weekly Insulin Icodec vs Once-Daily Insulin Degludec in Adults With Insulin-Naive Type 2 Diabetes: The ONWARDS 3 Randomized Clinical Trial | 2023 | 26-week phase 3a randomised double-blind double-dummy treat-to-target trial, n=588 insulin-naive adults with type 2 diabetes | PMID DOI | |
| Insulin icodec | Switching to once-weekly insulin icodec versus once-daily insulin glargine U100 in individuals with basal-bolus insulin-treated type 2 diabetes (ONWARDS 4): a phase 3a, randomised, open-label, multicentre, treat-to-target, non-inferiority trial | 2023 | 26-week phase 3a randomised open-label treat-to-target non-inferiority trial, n=582 adults with type 2 diabetes on basal-bolus therapy | PMID | |
| Insulin icodec | Once-Weekly Insulin Icodec With Dosing Guide App Versus Once-Daily Basal Insulin Analogues in Insulin-Naive Type 2 Diabetes (ONWARDS 5): A Randomized Trial | 2023 | 52-week pragmatic randomised open-label trial, n=1,085 insulin-naive adults with type 2 diabetes | PMID DOI | |
| Insulin icodec | Once-weekly insulin icodec versus once-daily insulin degludec as part of a basal-bolus regimen in individuals with type 1 diabetes (ONWARDS 6): a phase 3a, randomised, open-label, treat-to-target trial | 2023 | 52-week phase 3a randomised open-label treat-to-target trial with the primary endpoint at week 26, n=582 adults with type 1 diabetes on basal-bolus therapy (icodec n=290, degludec n=292) | PMID DOI | |
| Insulin icodec | Molecular Engineering of Insulin Icodec, the First Acylated Insulin Analog for Once-Weekly Administration in Humans | 2021 | Preclinical and early clinical molecular pharmacology | PMID DOI | |
| Insulin lispro | Reduction of postprandial hyperglycemia and frequency of hypoglycemia in IDDM patients on insulin-analog treatment | 1997 | Randomised open-label crossover trial, n=1,008 adults with type 1 diabetes, multinational, six months per treatment | PMID DOI | |
| Insulin lispro | Insulin lispro in CSII: results of a double-blind crossover study | 1997 | Double-blind randomised crossover trial of continuous subcutaneous insulin infusion, lispro versus regular human insulin | PMID | |
| Insulin lispro | Short-acting insulin analogues versus regular human insulin for adults with type 1 diabetes mellitus | 2016 | Systematic review and meta-analysis of randomised controlled trials in adults with type 1 diabetes | PMID DOI | |
| Insulin lispro | Efficacy and Safety of Rapid-Acting Insulin Analogs in Special Populations with Type 1 Diabetes or Gestational Diabetes: Systematic Review and Meta-Analysis | 2018 | Systematic review and meta-analysis covering pregnancy, paediatric populations and pump therapy | PMID | |
| Ipamorelin | Ipamorelin, the first selective growth hormone secretagogue | 1998 | In vitro and in vivo characterisation in rat pituitary cells, rats and swine | Preclinical only | PMID DOI |
| Ipamorelin | Pharmacokinetic-pharmacodynamic modeling of ipamorelin, a growth hormone releasing peptide, in human volunteers | 1999 | Dose-escalation pharmacokinetic-pharmacodynamic study in healthy male volunteers, intravenous infusion | Limited evidence | PMID DOI |
| Ipamorelin | Prospective, randomized, controlled, proof-of-concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients | 2014 | Multicentre, double-blind, placebo-controlled phase 2 trial in adults undergoing open or laparoscopic bowel resection; 117 enrolled, 114 treated; intravenous ipamorelin 0.03 mg/kg twice daily from postoperative day 1 to day 7 or discharge | Mixed evidence | PMID DOI Trial |
| Ipamorelin | A receptor in pituitary and hypothalamus that functions in growth hormone release | 1996 | Molecular cloning and characterisation of the growth hormone secretagogue receptor | Preclinical only | PMID DOI |
| Isophane insulin (NPH) | The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus | 1993 | Randomised controlled trial, n=1,441 people with type 1 diabetes, mean follow-up 6.5 years, intensive versus conventional therapy using regular human insulin and isophane insulin | PMID DOI | |
| Isophane insulin (NPH) | Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33) | 1998 | Randomised controlled trial, n=3,867 people with newly diagnosed type 2 diabetes, median 10 years' follow-up | PMID | |
| Isophane insulin (NPH) | Long-acting insulin analogues versus NPH insulin (human isophane insulin) for type 2 diabetes mellitus | 2007 | Systematic review and meta-analysis of randomised controlled trials | PMID DOI | |
| Isophane insulin (NPH) | Association of Initiation of Basal Insulin Analogs vs Neutral Protamine Hagedorn Insulin With Hypoglycemia-Related Emergency Department Visits or Hospital Admissions and With Glycemic Control in Patients With Type 2 Diabetes | 2018 | Retrospective observational cohort with propensity-score matching, n=25,489 adults with type 2 diabetes initiating basal insulin in an integrated health system | PMID DOI | |
| Isophane insulin (NPH) | The treat-to-target trial: randomized addition of glargine or human NPH insulin to oral therapy of type 2 diabetic patients | 2003 | 24-week randomised open-label parallel-group treat-to-target trial, n=756 adults with type 2 diabetes | PMID DOI | |
| ixazomib | Oral ixazomib, lenalidomide, and dexamethasone for multiple myeloma | 2016 | Randomised double-blind placebo-controlled phase 3, 722 patients with relapsed/refractory myeloma | PMID DOI | |
| ixazomib | Final overall survival analysis of the TOURMALINE-MM1 phase III trial of ixazomib, lenalidomide, and dexamethasone in patients with relapsed or refractory multiple myeloma | 2021 | Pre-specified final overall survival analysis of TOURMALINE-MM1 after median follow-up of approximately 85 months | PMID DOI | |
| ixazomib | Oral ixazomib maintenance following autologous stem cell transplantation (TOURMALINE-MM3): a double-blind, randomised, placebo-controlled phase 3 trial | 2019 | Randomised double-blind placebo-controlled phase 3, 656 patients randomised 3:2 to ixazomib or placebo maintenance after autologous transplantation | PMID DOI | |
| Kisspeptin-10 | Kisspeptin-10 is a potent stimulator of LH and increases pulse frequency in men | 2011 | Human physiological study in healthy men: intravenous kisspeptin-10 boluses (0.01-3.0 micrograms/kg) and continuous infusions up to 22.5 hours, with deconvolution analysis of LH secretion | Limited evidence | PMID DOI |
| Kisspeptin-10 | Kisspeptin Responsiveness Signals Emergence of Reproductive Endocrine Activity: Implications for Human Puberty | 2016 | Human physiological study in six men with idiopathic hypogonadotropic hypogonadism who had undergone spontaneous reversal, comparing kisspeptin responsiveness in those sustaining versus relapsing from reversal | Limited evidence | PMID DOI |
| Kisspeptin-10 | Kisspeptin modulates sexual and emotional brain processing in humans | 2017 | Randomised, double-blind, placebo-controlled two-way crossover fMRI study, n=29 healthy heterosexual young men, 75-minute intravenous infusion of kisspeptin-54 at 1 nmol/kg/hour | Mixed evidence | PMID DOI |
| Kisspeptin-10 | Modulations of human resting brain connectivity by kisspeptin enhance sexual and emotional functions | 2018 | Randomised, double-blind, placebo-controlled two-way crossover resting-state fMRI study, n=29 healthy men, intravenous kisspeptin-54 | Mixed evidence | PMID DOI |
| Kisspeptin-10 | Effects of Kisspeptin Administration in Women With Hypoactive Sexual Desire Disorder: A Randomized Clinical Trial | 2022 | Double-masked, placebo-controlled two-way crossover randomised trial; 40 premenopausal women with HSDD randomised, 32 completed both visits; single 75-minute intravenous kisspeptin-54 infusion | Mixed evidence | PMID DOI |
| Kisspeptin-10 | Effects of Kisspeptin on Sexual Brain Processing and Penile Tumescence in Men With Hypoactive Sexual Desire Disorder: A Randomized Clinical Trial | 2023 | Double-blind, placebo-controlled two-way crossover randomised trial; 37 men with HSDD randomised, 32 completed; single 75-minute intravenous kisspeptin-54 infusion | Mixed evidence | PMID DOI |
| Kisspeptin-54 | Kisspeptin-54 triggers egg maturation in women undergoing in vitro fertilization | 2014 | Single-centre proof-of-concept dose-ranging study, 53 women undergoing IVF, single subcutaneous kisspeptin-54 injection as oocyte maturation trigger | PMID | |
| Kisspeptin-54 | Efficacy of Kisspeptin-54 to Trigger Oocyte Maturation in Women at High Risk of Ovarian Hyperstimulation Syndrome (OHSS) During In Vitro Fertilization (IVF) Therapy | 2015 | Single-centre study of kisspeptin-54 as oocyte maturation trigger in 60 women at high risk of ovarian hyperstimulation syndrome | PMID | |
| Kisspeptin-54 | Increasing LH pulsatility in women with hypothalamic amenorrhoea using intravenous infusion of Kisspeptin-54 | 2014 | Single-blinded controlled crossover study, five women with hypothalamic amenorrhoea, six visits each receiving eight-hour infusions of vehicle or one of five kisspeptin-54 doses (0.01 to 1.00 nmol/kg/h) | PMID | |
| KPV (lysyl-prolyl-valine) | PepT1-mediated tripeptide KPV uptake reduces intestinal inflammation | 2008 | Human intestinal epithelial cell lines and mouse colitis models | Preclinical only | PMID DOI |
| KPV (lysyl-prolyl-valine) | Melanocortin-derived tripeptide KPV has anti-inflammatory potential in murine models of inflammatory bowel disease | 2008 | Two mouse colitis models (DSS and CD45RB-high transfer), plus MC1R-deficient mice | Preclinical only | PMID DOI |
| KPV (lysyl-prolyl-valine) | Dissection of the anti-inflammatory effect of the core and C-terminal (KPV) alpha-melanocyte-stimulating hormone peptides | 2003 | Rodent inflammation models comparing alpha-MSH fragments | Preclinical only | PMID DOI |
| KPV (lysyl-prolyl-valine) | Orally Targeted Delivery of Tripeptide KPV via Hyaluronic Acid-Functionalized Nanoparticles Efficiently Alleviates Ulcerative Colitis | 2017 | Mouse ulcerative colitis model with engineered oral nanoparticle delivery | Preclinical only | PMID DOI |
| KPV (lysyl-prolyl-valine) | Inhibition of cellular and systemic inflammation cues in human bronchial epithelial cells by melanocortin-related peptides: mechanism of KPV action and a role for MC3R agonists | 2012 | Immortalised human bronchial epithelial cell culture (16HBE14o-), measuring TNF-alpha- and RSV-evoked NF-kappaB signalling | Preclinical only | PMID |
| Lanreotide | Lanreotide in metastatic enteropancreatic neuroendocrine tumors | 2014 | Randomised, double-blind, placebo-controlled multinational phase 3 trial in 204 patients with metastatic grade 1 or 2 (Ki-67 up to 10%) non-functioning enteropancreatic neuroendocrine tumours; lanreotide autogel 120 mg or placebo every 28 days for 96 weeks | PMID DOI Trial | |
| Lanreotide | Lanreotide autogel/depot in advanced enteropancreatic neuroendocrine tumours: final results of the CLARINET open-label extension study | 2021 | Open-label extension of the CLARINET phase 3 trial; 89 patients took part (42 previously on lanreotide, 47 previously on placebo) | PMID DOI | |
| Lanreotide | Evaluation of lanreotide depot/autogel efficacy and safety as a carcinoid syndrome treatment (ELECT): a randomized, double-blind, placebo-controlled trial | 2016 | Phase 3 randomised, double-blind, placebo-controlled 16-week trial in 115 patients with carcinoid syndrome (lanreotide 59, placebo 56), with the percentage of days requiring rescue short-acting octreotide as the primary endpoint | PMID DOI | |
| Lanreotide | Comparison of octreotide acetate LAR and lanreotide SR in patients with acromegaly | 2000 | Multicentre switch study in 125 patients with acromegaly previously on lanreotide SR 30 mg every 10 or 14 days, switched to octreotide LAR 20 mg monthly; the timing of the switch was randomised 3:1, not the drug allocation | PMID DOI | |
| Lepirudin | Lepirudin (recombinant hirudin) for parenteral anticoagulation in patients with heparin-induced thrombocytopenia | 1999 | Prospective multicentre cohort study with a historical control group; 95 lepirudin-treated patients with confirmed heparin-induced thrombocytopenia compared with 120 historical control patients | PMID DOI | |
| Lepirudin | Heparin-induced thrombocytopenia with thromboembolic complications: meta-analysis of 2 prospective trials to assess the value of parenteral treatment with lepirudin and its therapeutic aPTT range | 2000 | Meta-analysis of two prospective trials; 113 lepirudin-treated patients compared with 91 historical control patients | PMID | |
| Lepirudin | Anaphylactic and anaphylactoid reactions associated with lepirudin in patients with heparin-induced thrombocytopenia | 2003 | Pharmacovigilance analysis of spontaneously reported severe reactions across approximately 35,000 lepirudin-treated patients | PMID | |
| Leu-enkephalin | Identification of two related pentapeptides from the brain with potent opiate agonist activity | 1975 | Peptide isolation, sequencing and bioassay | PMID | |
| Leu-enkephalin | Racecadotril for acute diarrhoea in children | 2019 | Systematic review and meta-analysis of seven randomised trials, approximately 1,140 children | PMID DOI | |
| Leu-enkephalin | Dynorphin is a specific endogenous ligand of the kappa opioid receptor | 1982 | Receptor binding and bioassay characterisation | PMID DOI | |
| Leuprorelin | Leuprolide versus diethylstilbestrol for metastatic prostate cancer | 1984 | Multicentre randomised controlled trial, 199 men with previously untreated metastatic prostate cancer | PMID | |
| Leuprorelin | Relative effectiveness and cost-effectiveness of methods of androgen suppression in the treatment of advanced prostate cancer | 1999 | Systematic review and meta-analysis of randomised trials of androgen suppression methods | PMID | |
| Leuprorelin | The efficacy and safety of degarelix: a 12-month, comparative, randomized, open-label, parallel-group phase III study in patients with prostate cancer | 2008 | Randomised open-label phase 3 trial (CS21), 610 men, degarelix versus leuprorelin 7.5 mg monthly | PMID | |
| Leuprorelin | Cardiovascular Safety of Degarelix Versus Leuprolide in Patients With Prostate Cancer: The Primary Results of the PRONOUNCE Randomized Trial | 2021 | Randomised open-label trial, 545 men with prostate cancer and established cardiovascular disease | PMID Trial | |
| Linaclotide | Two randomized trials of linaclotide for chronic constipation | 2011 | Two identical phase 3 randomised, double-blind, placebo-controlled trials (trials 303 and 01), 1,276 patients, 12 weeks | PMID | |
| Linaclotide | Linaclotide for irritable bowel syndrome with constipation: a 26-week, randomized, double-blind, placebo-controlled trial to evaluate efficacy and safety | 2012 | Phase 3 randomised, double-blind, parallel-group, placebo-controlled trial, 804 patients, 26 weeks | PMID | |
| Linaclotide | A 12-week, randomized, controlled trial with a 4-week randomized withdrawal period to evaluate the efficacy and safety of linaclotide in irritable bowel syndrome with constipation | 2012 | Phase 3 randomised, double-blind, placebo-controlled trial with 4-week randomised withdrawal, 800 patients, 12 weeks | PMID | |
| Linaclotide | Randomised clinical trials: linaclotide phase 3 studies in IBS-C, a prespecified further analysis based on European Medicines Agency-specified endpoints | 2013 | Prespecified pooled reanalysis of two phase 3 trials (n=803 and n=805 as randomised in that analysis) using EMA-specified co-primary responder definitions | PMID | |
| Liraglutide | Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes | 2016 | Randomised, double-blind, placebo-controlled cardiovascular outcome trial, n=9,341, median follow-up 3.8 years | High-quality evidence | PMID DOI Trial |
| Liraglutide | A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management | 2015 | Randomised, double-blind, placebo-controlled phase 3 trial, n=3,731, 56 weeks | High-quality evidence | PMID DOI Trial |
| Liraglutide | Efficacy of Liraglutide for Weight Loss Among Patients With Type 2 Diabetes: The SCALE Diabetes Randomized Clinical Trial | 2015 | Randomised, double-blind, placebo-controlled trial, n=846, 56 weeks | High-quality evidence | PMID DOI |
| Lixisenatide | Efficacy and safety of the once-daily GLP-1 receptor agonist lixisenatide in monotherapy: a randomized, double-blind, placebo-controlled trial in patients with type 2 diabetes (GetGoal-Mono) | 2012 | 12-week randomised, double-blind, placebo-controlled phase 3 monotherapy trial, 361 adults across two titration regimens and pooled placebo | PMID DOI | |
| Lixisenatide | Adding once-daily lixisenatide for type 2 diabetes inadequately controlled by established basal insulin: a 24-week, randomized, placebo-controlled comparison (GetGoal-L) | 2013 | 24-week randomised, double-blind, parallel-group, placebo-controlled trial, 495 adults on established basal insulin | PMID DOI | |
| Lixisenatide | Lixisenatide in Patients with Type 2 Diabetes and Acute Coronary Syndrome | 2015 | Randomised, double-blind, placebo-controlled cardiovascular outcomes trial, 6,068 participants with recent acute coronary syndrome, median follow-up 25 months | PMID DOI Trial | |
| LL-37 | Treatment with LL-37 is safe and effective in enhancing healing of hard-to-heal venous leg ulcers: a randomized, placebo-controlled clinical trial | 2014 | First-in-human phase I/IIa; n=34; 3-week placebo run-in, then 4 weeks of twice-weekly topical LL-37 at 0.5, 1.6 or 3.2 mg/mL versus placebo, plus 4-week follow-up; volume 22(5):613-621 | Mixed evidence | PMID DOI |
| LL-37 | Evaluation of LL-37 in healing of hard-to-heal venous leg ulcers: A multicentric prospective randomized placebo-controlled clinical trial | 2021 | Phase IIb, double-blind, randomised, placebo-controlled, parallel-group trial at sites in Poland and Sweden; 148 patients treated; topical LL-37 at 0.5 or 1.6 mg/mL twice weekly alongside compression therapy; volume 29(6):938-950 | High-quality evidence | PMID DOI |
| LL-37 | Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide | 2007 | Mechanistic study in human cells and psoriatic skin; volume 449(7162):564-569 | Preclinical only | PMID DOI |
| LL-37 | The antimicrobial peptide LL37 is a T-cell autoantigen in psoriasis | 2014 | Human immunological study of circulating and skin-derived T cells from patients with moderate-to-severe plaque psoriasis; volume 5, article 5621 | Preclinical only | PMID DOI |
| Long R3 IGF-1 (LR3-IGF-1) | Novel recombinant fusion protein analogues of insulin-like growth factor (IGF)-I indicate the relative importance of IGF-binding protein and receptor binding for enhanced biological potency | 1992 | In vitro characterisation of N-terminally extended IGF-1 fusion analogues, including Long [Arg3]-IGF-I, across L6 myoblasts, H35 hepatoma cells and chicken embryo fibroblasts | Preclinical only | PMID DOI |
| Long R3 IGF-1 (LR3-IGF-1) | Production and characterization of recombinant insulin-like growth factor-I (IGF-I) and potent analogues of IGF-I, with Gly or Arg substituted for Glu3, following their expression in Escherichia coli as fusion proteins | 1992 | Recombinant expression, folding and biochemical characterisation of IGF-1 and its Gly3 and Arg3 analogues in E. coli | Preclinical only | PMID DOI |
| Long R3 IGF-1 (LR3-IGF-1) | Insulin-like growth factor-I (IGF-I) and especially IGF-I variants are anabolic in dexamethasone-treated rats | 1992 | Controlled infusion study in glucocorticoid-treated rats | Preclinical only | PMID DOI |
| Long R3 IGF-1 (LR3-IGF-1) | Long R3 insulin-like growth factor-I (IGF-I) infusion stimulates organ growth but reduces plasma IGF-I, IGF-II and IGF binding protein concentrations in the guinea pig | 1995 | Continuous infusion study in guinea pigs | Preclinical only | PMID DOI |
| Long R3 IGF-1 (LR3-IGF-1) | The somatotropic axis in neonatal calves can be modulated by nutrition, growth hormone, and Long-R3-IGF-I | 1997 | Controlled feeding and hormone administration study in neonatal calves | Preclinical only | PMID DOI |
| Long R3 IGF-1 (LR3-IGF-1) | Detection of His-tagged Long-R3-IGF-I in a black market product | 2010 | Analytical characterisation of a seized injection vial by immunoaffinity purification, nano-UPLC mass spectrometry and ELISA | Limited evidence | PMID DOI |
| lutetium (177Lu) oxodotreotide | Phase 3 trial of 177Lu-Dotatate for midgut neuroendocrine tumors | 2017 | Randomised open-label phase 3, 229 patients with advanced progressive somatostatin-receptor-positive midgut neuroendocrine tumours | PMID DOI | |
| lutetium (177Lu) oxodotreotide | 177Lu-Dotatate plus long-acting octreotide versus high-dose long-acting octreotide in patients with midgut neuroendocrine tumours (NETTER-1): final overall survival and long-term safety results from an open-label, randomised, controlled, phase 3 trial | 2021 | Final overall survival analysis of NETTER-1 at median follow-up over six years | PMID DOI | |
| lutetium (177Lu) oxodotreotide | [177Lu]Lu-DOTA-TATE plus long-acting octreotide versus high-dose long-acting octreotide for the treatment of newly diagnosed, advanced grade 2-3, well-differentiated, gastroenteropancreatic neuroendocrine tumours (NETTER-2): an open-label, randomised, phase 3 study | 2024 | Randomised open-label phase 3, 226 patients with newly diagnosed advanced grade 2-3 gastroenteropancreatic neuroendocrine tumours, first-line setting | PMID DOI | |
| lutetium (177Lu) oxodotreotide | Long-term efficacy, survival, and safety of [177Lu-DOTA0,Tyr3]octreotate in patients with gastroenteropancreatic and bronchial neuroendocrine tumors | 2017 | Large single-centre observational cohort, 610 patients treated at Erasmus Medical Centre with long-term follow-up | PMID DOI | |
| lutetium (177Lu) vipivotide tetraxetan | Lutetium-177-PSMA-617 for metastatic castration-resistant prostate cancer | 2021 | Randomised open-label phase 3, 831 patients with PSMA-positive mCRPC previously treated with an androgen receptor pathway inhibitor and taxane chemotherapy | PMID DOI | |
| lutetium (177Lu) vipivotide tetraxetan | [177Lu]Lu-PSMA-617 versus cabazitaxel in patients with metastatic castration-resistant prostate cancer (TheraP): a randomised, open-label, phase 2 trial | 2021 | Randomised open-label phase 2 head-to-head comparison against cabazitaxel chemotherapy, 200 men | PMID DOI | |
| lutetium (177Lu) vipivotide tetraxetan | Overall survival with [177Lu]Lu-PSMA-617 versus cabazitaxel in metastatic castration-resistant prostate cancer (TheraP): secondary outcomes of a randomised, open-label, phase 2 trial | 2024 | Secondary overall survival analysis of the TheraP randomised phase 2 trial | PMID DOI | |
| lutetium (177Lu) vipivotide tetraxetan | 177Lu-PSMA-617 versus a change of androgen receptor pathway inhibitor therapy for taxane-naive patients with progressive metastatic castration-resistant prostate cancer (PSMAfore): a phase 3, randomised, controlled trial | 2024 | Randomised open-label phase 3, 468 taxane-naive patients randomised to the radioligand or a switch of androgen receptor pathway inhibitor | PMID DOI | |
| Macimorelin | Macimorelin as a Diagnostic Test for Adult GH Deficiency | 2018 | Multicentre, open-label, randomised, two-way crossover trial comparing single-dose oral macimorelin with the insulin tolerance test. The efficacy analysis included subjects at high (n=38), intermediate (n=37) and low (n=39) likelihood of adult growth hormone deficiency plus 25 matched healthy controls | PMID DOI | |
| Macimorelin | European Medicines Agency marketing authorisation record: macimorelin for the diagnosis of growth hormone deficiency in adults | 2019 | EU regulatory assessment and authorisation record for macimorelin | none | |
| Macimorelin | Molecular recognition of two approved drugs Macimorelin and Anamorelin by the growth hormone secretagogue receptor | 2025 | Cryo-electron microscopy structures of GHS-R1a bound to macimorelin and to anamorelin in complex with Gq proteins, at 2.63 and 2.52 angstrom resolution, with systematic mutagenesis and functional assays | PMID DOI | |
| Mazdutide | A phase 1b randomised controlled trial of a glucagon-like peptide-1 and glucagon receptor dual agonist IBI362 (LY3305677) in Chinese patients with type 2 diabetes | 2022 | Randomised, placebo-controlled, multiple-ascending-dose phase 1b trial in 43 Chinese adults with type 2 diabetes across nine centres; 12 weeks of once-weekly IBI362 at 3.0, 4.5 or 6.0 mg, placebo, or dulaglutide; 42 completed | PMID | |
| Mazdutide | A phase 2 randomised controlled trial of mazdutide in Chinese overweight adults or adults with obesity | 2023 | 24-week randomised, double-blind, placebo-controlled phase 2 trial in 248 Chinese adults with overweight or obesity across 20 hospitals | PMID | |
| Mazdutide | Efficacy and Safety of Mazdutide in Chinese Patients With Type 2 Diabetes: A Randomized, Double-Blind, Placebo-Controlled Phase 2 Trial | 2024 | Randomised, double-blind, placebo-controlled phase 2 trial in Chinese adults with type 2 diabetes | PMID | |
| Mazdutide | Once-Weekly Mazdutide in Chinese Adults with Obesity or Overweight | 2025 | 48-week randomised, double-blind, placebo-controlled phase 3 trial, 610 Chinese adults with BMI at least 28, or 24-28 with an obesity-related comorbidity; mean baseline weight 87.2 kg, mean BMI 31.1 | PMID DOI | |
| Mazdutide | Mazdutide versus placebo in Chinese adults with type 2 diabetes | 2026 | 24-week randomised, double-blind, placebo-controlled phase 3 trial in just over 300 Chinese adults with type 2 diabetes | PMID DOI | |
| Mazdutide | Mazdutide versus dulaglutide in Chinese adults with type 2 diabetes | 2026 | Randomised active-comparator phase 3 trial of mazdutide 4 mg and 6 mg against dulaglutide in Chinese adults with type 2 diabetes | PMID | |
| Mechano growth factor (IGF-1Ec E-peptide) | Cloning and characterization of an IGF-1 isoform expressed in skeletal muscle subjected to stretch | 1996 | Molecular cloning from mechanically stretched rabbit skeletal muscle | Preclinical only | PMID DOI |
| Mechano growth factor (IGF-1Ec E-peptide) | Expression of insulin growth factor-1 splice variants and structural genes in rabbit skeletal muscle induced by stretch and stimulation | 1999 | Controlled stretch and electrical stimulation of rabbit skeletal muscle with transcript quantification | Preclinical only | PMID DOI |
| Mechano growth factor (IGF-1Ec E-peptide) | Minireview: Mechano-growth factor: a putative product of IGF-I gene expression involved in tissue repair and regeneration | 2010 | Critical review of the MGF literature | Preclinical only | PMID DOI |
| Mechano growth factor (IGF-1Ec E-peptide) | Insulin-like growth factor-I E-peptide activity is dependent on the IGF-I receptor | 2012 | Receptor-dependence experiments in cultured muscle cells using IGF-1R blockade and knockdown | Preclinical only | PMID DOI |
| Mechano growth factor (IGF-1Ec E-peptide) | Mechano Growth Factor E peptide (MGF-E), derived from an isoform of IGF-1, activates human muscle progenitor cells and induces an increase in their fusion potential at different ages | 2011 | In vitro treatment of human muscle progenitor cells from young and elderly donors | Preclinical only | PMID DOI |
| Mechano growth factor (IGF-1Ec E-peptide) | Mass spectrometric characterization of a biotechnologically produced full-length mechano growth factor (MGF) relevant for doping controls | 2014 | Analytical characterisation by mass spectrometry of commercially produced full-length MGF | Limited evidence | PMID DOI |
| Mechano growth factor (IGF-1Ec E-peptide) | Detection and in vitro metabolism of the confiscated peptides BPC 157 and MGF R23H | 2017 | Analytical characterisation and in vitro metabolic stability testing of peptides seized from the black market | Limited evidence | PMID DOI |
| Melanotan II | Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study | 1996 | Uncontrolled pilot phase I study in 3 healthy male volunteers, escalating subcutaneous doses of 0.01-0.03 mg/kg over two weeks | Limited evidence | PMID |
| Melanotan II | Synthetic melanotropic peptide initiates erections in men with psychogenic erectile dysfunction: double-blind, placebo controlled crossover study | 1998 | Double-blind, placebo-controlled crossover trial, n=10 men with erectile dysfunction of psychogenic origin | Limited evidence | PMID |
| Melanotan II | Effect of an alpha-melanocyte stimulating hormone analog on penile erection and sexual desire in men with organic erectile dysfunction | 2000 | Double-blind, placebo-controlled crossover trial, n=10 men with organic erectile dysfunction | Limited evidence | PMID DOI |
| Melanotan II | Melanotan II injection resulting in systemic toxicity and rhabdomyolysis | 2012 | Single case report - 39-year-old man who self-injected 6 mg of melanotan II purchased online | Limited evidence | PMID DOI |
| Melanotan II | Melanoma associated with the use of melanotan-II | 2014 | Single case report | Limited evidence | PMID DOI |
| Melanotan II | Melanotan-associated melanoma | 2011 | Single case report (letter) | Limited evidence | PMID DOI |
| Met-enkephalin | Identification of two related pentapeptides from the brain with potent opiate agonist activity | 1975 | Peptide isolation, sequencing and bioassay from porcine brain | PMID | |
| Met-enkephalin | Racecadotril for acute diarrhoea in children | 2019 | Systematic review and meta-analysis of seven randomised trials, approximately 1,140 children | PMID DOI | |
| Met-enkephalin | Opioid growth factor improves clinical benefit and survival in patients with advanced pancreatic cancer | 2010 | Prospective open-label single-arm phase 2 trial, 24 patients who had failed standard chemotherapy, compared with historical controls | PMID DOI | |
| Motilin | Receptor for motilin identified in the human gastrointestinal system | 1999 | Receptor cloning and pharmacological characterisation in human tissue | PMID DOI | |
| Motilin | Sequence of an intestinal cDNA encoding human motilin precursor | 1987 | Molecular cloning | PMID DOI | |
| Motilin | GSK962040: a small molecule, selective motilin receptor agonist, effective as a stimulant of human and rabbit gastrointestinal motility | 2009 | Preclinical and human tissue pharmacology | Preclinical only | PMID DOI |
| Motilin | The effect of camicinal (GSK962040), a motilin agonist, on gastric emptying and glucose absorption in feed-intolerant critically ill patients: a randomized, blinded, placebo-controlled, clinical trial | 2016 | Prospective randomised, double-blind, parallel-group, placebo-controlled trial, 23 mechanically ventilated feed-intolerant patients (camicinal 50 mg n=15, placebo n=8), single dose | PMID DOI | |
| Motilin | Manometric evaluation of the motilin receptor agonist camicinal (GSK962040) in humans | 2018 | Randomised, double-blind, crossover controlled human antroduodenal manometry study | PMID | |
| MOTS-c | The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis and reduces obesity and insulin resistance | 2015 | Preclinical; cell culture and mouse models including high-fat-diet and aged mice | Preclinical only | PMID DOI |
| MOTS-c | MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis | 2021 | Preclinical mouse studies with supporting human exercise sampling | Preclinical only | PMID DOI |
| MOTS-c | The mitochondrial-derived peptide MOTS-c: a player in exceptional longevity? | 2015 | Genetic association study in Japanese cohorts including centenarians | Limited evidence | PMID DOI |
| MOTS-c | A pro-diabetogenic mtDNA polymorphism in the mitochondrial-derived peptide, MOTS-c | 2021 | Genetic association study with supporting functional work | Limited evidence | PMID DOI |
| MOTS-c | MOTS-c modulates skeletal muscle function by directly binding and activating CK2 | 2024 | Preclinical; biochemical binding studies and rodent skeletal muscle | Preclinical only | PMID DOI |
| MOTS-c | MOTS-c for Improving Insulin Sensitivity in Adults With Prediabetes and Overweight/Obesity | 2026 | Phase 2a, randomised, double-blind, placebo-controlled interventional trial, planned n=120, 12 weeks | Limited evidence | Trial |
| Myostatin (GDF-8) | Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member | 1997 | Gene targeting and phenotypic characterisation of myostatin-null mice | Preclinical only | PMID DOI |
| Myostatin (GDF-8) | Myostatin mutation associated with gross muscle hypertrophy in a child | 2004 | Clinical and genetic case report with family segregation analysis | Limited evidence | PMID DOI |
| Myostatin (GDF-8) | Regulation of muscle growth by multiple ligands signaling through activin type II receptors | 2005 | Soluble ActRIIB administration in wild-type and myostatin-null mice | Preclinical only | PMID DOI |
| Myostatin (GDF-8) | A phase I/II trial of MYO-029 in adult subjects with muscular dystrophy | 2008 | Randomised, double-blind, placebo-controlled dose-escalation in adults with Becker, facioscapulohumeral and limb-girdle muscular dystrophies | Mixed evidence | PMID DOI |
| Myostatin (GDF-8) | Bimagrumab vs Optimized Standard of Care for Treatment of Sarcopenia in Community-Dwelling Older Adults: A Randomized Clinical Trial | 2020 | Randomised, double-blind, placebo-controlled trial in community-dwelling older adults with sarcopenia | Mixed evidence | PMID DOI |
| Myostatin (GDF-8) | Effect of Bimagrumab vs Placebo on Body Fat Mass Among Adults With Type 2 Diabetes and Obesity: A Phase 2 Randomized Clinical Trial | 2021 | Phase 2 randomised, double-blind, placebo-controlled trial in adults with type 2 diabetes and obesity | Mixed evidence | PMID DOI |
| Myostatin (GDF-8) | Safety and efficacy of apitegromab in nonambulatory type 2 or type 3 spinal muscular atrophy (SAPPHIRE): a phase 3, double-blind, randomised, placebo-controlled trial | 2025 | Phase 3 randomised, double-blind, placebo-controlled trial; 188 patients enrolled in total, comprising a main efficacy population of 156 aged 2-12 randomised 1:1:1 to apitegromab 10 mg/kg, 20 mg/kg or placebo intravenously every 4 weeks for 12 months on background SMN-targeted therapy, plus an exploratory cohort of 32 aged 13-21 | High-quality evidence | PMID DOI |
| myristoyl pentapeptide-17 | Collagen stimulating effect of peptide amphiphile C16-KTTKS on human fibroblasts | 2013 | Biophysical characterisation plus fibroblast culture | Preclinical only | PMID |
| myristoyl pentapeptide-17 | Noninvasive Monitoring of Palmitoyl Hexapeptide-12 in Human Skin Layers: Mechanical Interaction with Skin Components and Its Potential Skincare Benefits | 2025 | Label-free analytical study (orbital trapping secondary ion mass spectrometry, stimulated Raman scattering) on full-thickness human skin | Preclinical only | PMID DOI |
| myristoyl pentapeptide-17 | Complications and adverse effects of periocular aesthetic treatments | 2022 | Narrative review | PMID | |
| N-Acetyl Epitalon | Epithalon peptide induces telomerase activity and telomere elongation in human somatic cells | 2003 | In vitro, telomerase-negative human fetal fibroblast culture | Preclinical only | PMID DOI |
| N-Acetyl semax amidate | N-terminal degradation of ACTH(4-10) and its synthetic analog semax by the rat blood enzymes | 1991 | In vitro enzymatic degradation study in rat blood | Preclinical only | PMID DOI |
| N-Acetyl semax amidate | Degradation of the ACTH(4-10) analog Semax in the presence of rat basal forebrain cell cultures and plasma membranes | 2006 | In vitro degradation of labelled Semax by rat basal forebrain cultures and plasma membranes | Preclinical only | PMID DOI |
| N-Acetyl semax amidate | Kinetics of Semax penetration into the brain and blood of rats after its intranasal administration | 2006 | Pharmacokinetic study of labelled Semax in rats after intranasal administration | Preclinical only | PMID DOI |
| Nafarelin | Administration of nasal nafarelin as compared with oral danazol for endometriosis. A multicenter double-blind comparative clinical trial | 1988 | Multicentre double-blind double-dummy randomised controlled trial, nafarelin nasal spray versus oral danazol in laparoscopically confirmed endometriosis | PMID | |
| Nafarelin | A comparison of nafarelin acetate and danazol in the treatment of endometriosis | 1990 | Randomised comparative trial in women with endometriosis | PMID | |
| Nafarelin | Prospective randomized double-blind trial of 3 versus 6 months of nafarelin therapy for endometriosis associated pelvic pain | 1995 | Prospective randomised double-blind trial comparing treatment durations | PMID | |
| Nesiritide | Intravenous nesiritide, a natriuretic peptide, in the treatment of decompensated congestive heart failure | 2000 | Two parallel randomised trials totalling 432 patients: an efficacy trial in 127 patients (nesiritide versus placebo) and a comparative trial in 305 patients (nesiritide versus standard intravenous therapy) | PMID DOI | |
| Nesiritide | Intravenous nesiritide vs nitroglycerin for treatment of decompensated congestive heart failure: a randomized controlled trial | 2002 | Randomised, double-blind trial; 489 patients hospitalised with dyspnoea from decompensated heart failure (204 nesiritide, 143 nitroglycerin, 142 placebo) | PMID DOI | |
| Nesiritide | Risk of worsening renal function with nesiritide in patients with acutely decompensated heart failure | 2005 | Meta-analysis of 5 randomised controlled trials, 1,269 patients | PMID DOI | |
| Nesiritide | Effect of nesiritide in patients with acute decompensated heart failure | 2011 | Randomised, double-blind, placebo-controlled trial; 7,141 patients hospitalised with acute heart failure, nesiritide or placebo for 24-168 hours in addition to standard care | PMID DOI Trial | |
| Neuropeptide Y | Neuropeptide Y - a novel brain peptide with structural similarities to peptide YY and pancreatic polypeptide | 1982 | Peptide isolation and sequencing from porcine brain | PMID | |
| Neuropeptide Y | A Randomized Dose-Ranging Study of Neuropeptide Y in Patients with Posttraumatic Stress Disorder | 2018 | Double-blind randomised placebo-controlled crossover single-ascending-dose study across five dose cohorts; 26 randomised, 24 completed both treatment days | PMID DOI Trial | |
| Neuropeptide Y | A Randomized Controlled Trial of Intranasal Neuropeptide Y in Patients With Major Depressive Disorder | 2020 | Randomised double-blind placebo-controlled parallel-group trial, n=30 (12 NPY, 18 placebo), single 6.8 mg intranasal dose | PMID DOI | |
| Neuropeptide Y | Velneperit (S-2367), an oral neuropeptide Y Y5 receptor antagonist, in obesity | 2011 | Phase 2 randomised placebo-controlled trials in obesity | none | |
| Neurotensin | The isolation of a new hypotensive peptide, neurotensin, from bovine hypothalami | 1973 | Peptide isolation and characterisation | PMID | |
| Neurotensin | 177Lu-3BP-227 for Neurotensin Receptor 1-Targeted Therapy of Metastatic Pancreatic Adenocarcinoma: First Clinical Results | 2018 | First-in-human open-label uncontrolled case series, six patients | PMID | |
| Neurotensin | Study to Evaluate the Safety and Activity (Including Distribution) of 177Lu-3BP-227 in Subjects With Solid Tumours Expressing Neurotensin Receptor Type 1 | 2018 | Phase 1 open-label multicentre trial in NTSR1-expressing solid tumours including pancreatic, colorectal, gastric and head and neck cancer; registration status terminated | Trial | |
| Nicotinamide adenine dinucleotide (NAD+) | Chronic nicotinamide riboside supplementation is well-tolerated and elevates NAD+ in healthy middle-aged and older adults | 2018 | Randomised double-blind placebo-controlled crossover, n=30, 1000 mg/day NR for 6 weeks | Mixed evidence | PMID DOI |
| Nicotinamide adenine dinucleotide (NAD+) | A randomized placebo-controlled clinical trial of nicotinamide riboside in obese men: safety, insulin-sensitivity, and lipid-mobilizing effects | 2018 | Randomised double-blind placebo-controlled, n=40, 2000 mg/day NR for 12 weeks | High-quality evidence | PMID DOI |
| Nicotinamide adenine dinucleotide (NAD+) | Nicotinamide Riboside Augments the Aged Human Skeletal Muscle NAD+ Metabolome and Induces Transcriptomic and Anti-inflammatory Signatures | 2019 | Randomised double-blind placebo-controlled, aged men, 1000 mg/day NR for 21 days | Mixed evidence | PMID DOI |
| Nicotinamide adenine dinucleotide (NAD+) | Nicotinamide mononucleotide increases muscle insulin sensitivity in prediabetic women | 2021 | Randomised double-blind placebo-controlled, n=25, 250 mg/day NMN for 10 weeks, prediabetic postmenopausal women | Mixed evidence | PMID DOI |
| Nicotinamide adenine dinucleotide (NAD+) | The Effect of Nicotinamide Mononucleotide and Riboside on Skeletal Muscle Mass and Function: A Systematic Review and Meta-Analysis | 2025 | Systematic review and meta-analysis of randomised controlled trials | High-quality evidence | PMID DOI |
| Nicotinamide adenine dinucleotide (NAD+) | Effects of NAD+ precursors on blood pressure, C-reactive protein concentration and carotid intima-media thickness: A meta-analysis of randomized controlled trials | 2023 | Systematic review and meta-analysis of randomised controlled trials | High-quality evidence | PMID DOI |
| Nociceptin/orphanin FQ | Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor | 1995 | Peptide isolation and receptor deorphanisation | PMID | |
| Nociceptin/orphanin FQ | Orphanin FQ: a neuropeptide that activates an opioidlike G protein-coupled receptor | 1995 | Independent peptide isolation and receptor deorphanisation | PMID | |
| Nociceptin/orphanin FQ | A Selective Nociceptin Receptor Antagonist to Treat Depression: Evidence from Preclinical and Clinical Studies | 2016 | Preclinical pharmacology plus an eight-week randomised double-blind placebo-controlled proof-of-concept trial of LY2940094 40 mg once daily in major depressive disorder | PMID DOI | |
| Nociceptin/orphanin FQ | ALLEVIATE-1 and ALLEVIATE-2: cebranopadol for moderate-to-severe acute pain | 2025 | Two phase 3 randomised placebo-controlled trials in abdominoplasty and bunionectomy | none | |
| Obestatin | Obestatin, a peptide encoded by the ghrelin gene, opposes ghrelin's effects on food intake | 2005 | Rodent in vivo studies and in vitro receptor pharmacology | PMID | |
| Obestatin | GPR39 signaling is stimulated by zinc ions but not by obestatin | 2007 | Receptor pharmacology and signal transduction study | PMID | |
| Obestatin | Comment on 'Obestatin, a peptide encoded by the ghrelin gene, opposes ghrelin's effects on food intake' | 2007 | Technical comment challenging the original receptor assignment | PMID DOI | |
| Obestatin | Lack of obestatin effects on food intake: should obestatin be renamed ghrelin-associated peptide (GAP)? | 2007 | Review of rodent food intake, gastric transit and receptor-binding evidence | PMID | |
| Obestatin | Metabolic and structural properties of human obestatin {1-23} and two fragment peptides | 2010 | Rodent metabolic study with NMR structural characterisation | PMID DOI | |
| Octreotide | Treatment of the malignant carcinoid syndrome. Evaluation of a long-acting somatostatin analogue | 1986 | Uncontrolled open-label prospective evaluation of subcutaneous SMS 201-995, 150 micrograms three times daily, in 25 patients with histologically proved metastatic carcinoid tumours and carcinoid syndrome | PMID DOI | |
| Octreotide | Octreotide acetate long-acting formulation versus open-label subcutaneous octreotide acetate in malignant carcinoid syndrome | 1999 | Randomised trial comparing double-blinded octreotide LAR at 10, 20 and 30 mg every 4 weeks with open-label subcutaneous octreotide every 8 hours in carcinoid syndrome; 79 patients constituted the efficacy-assessable population | PMID DOI | |
| Octreotide | Placebo-controlled, double-blind, prospective, randomized study on the effect of octreotide LAR in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors: a report from the PROMID Study Group | 2009 | Randomised, double-blind, placebo-controlled phase 3 trial in 85 treatment-naive patients with metastatic well-differentiated midgut neuroendocrine tumours; octreotide LAR 30 mg intramuscularly every 28 days versus placebo | PMID DOI Trial | |
| Octreotide | Comparison of octreotide acetate LAR and lanreotide SR in patients with acromegaly | 2000 | Multicentre switch study in 125 patients with acromegaly at 26 centres in France, Spain and Germany, all previously on lanreotide SR 30 mg every 10 or 14 days, switched to octreotide LAR 20 mg monthly; the timing of the switch, not the drug, was randomised 3:1, with 27 patients continuing lanreotide SR for the first three months | PMID DOI | |
| Octreotide | Somatostatin analogues for acute bleeding oesophageal varices | 2008 | Systematic review and meta-analysis of 21 randomised trials including 2,588 patients with acute or recent bleeding from oesophageal varices, comparing somatostatin or its analogues with placebo or no treatment | PMID DOI | |
| Orexin A | Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior | 1998 | Orphan GPCR deorphanisation, peptide isolation, receptor cloning and pharmacological characterisation, with in vivo feeding studies | Preclinical only | PMID DOI |
| Orexin A | The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity | 1998 | Directional tag PCR subtraction to identify hypothalamus-specific transcripts, followed by electrophysiology in cultured neurons | Preclinical only | PMID DOI |
| Orexin A | Olfactory dysfunction in patients with narcolepsy with cataplexy is restored by intranasal Orexin A (Hypocretin-1) | 2008 | Olfactory testing in 10 narcolepsy-with-cataplexy patients versus 10 matched healthy controls, followed by a double-blind, randomised, placebo-controlled crossover of intranasal orexin A in seven of the patients with 2-phenyl-ethyl alcohol single-staircase odour detection thresholds | Limited evidence | PMID DOI |
| Orexin A | Effects of intranasal hypocretin-1 (orexin A) on sleep in narcolepsy with cataplexy | 2011 | Double-blind, random-order crossover, placebo-controlled, within-subject; n=8 patients with narcolepsy with cataplexy; 435 nmol intranasal human recombinant hypocretin-1 before night sleep followed by standard polysomnography | Limited evidence | PMID DOI |
| Orexin A | Orexin 2 receptor-selective agonist danavorexton improves narcolepsy phenotype in a mouse model and in human patients | 2022 | Orexin/ataxin-3 narcolepsy mouse work plus single- and multiple-rising-dose studies of intravenous danavorexton in healthy adults and in individuals with narcolepsy type 1 and type 2 | Mixed evidence | PMID DOI |
| Orexin B | Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior | 1998 | Peptide isolation, receptor cloning and binding pharmacology, with in vivo feeding studies | Preclinical only | PMID DOI |
| Orexin B | The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity | 1998 | Transcript subtraction to identify hypothalamus-specific peptides, followed by electrophysiology in cultured neurons | Preclinical only | PMID DOI |
| Orexin B | Structure and ligand-binding mechanism of the human OX1 and OX2 orexin receptors | 2016 | X-ray crystallography of human OX1R bound to the OX1R-selective antagonist SB-674042 and to the dual antagonist suvorexant, at 2.8 and 2.75 angstrom resolution, plus molecular modelling of OX2R selectivity | Preclinical only | PMID DOI |
| Orexin B | OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation without inducing drug-seeking behavior in mouse model of narcolepsy | 2022 | Orexin knockout mouse model; intracerebroventricular administration of the peptidic OX2R-selective agonist [Ala11, D-Leu15]-orexin-B versus orexin-A, with polysomnographic and behavioural endpoints | Preclinical only | PMID DOI |
| Orexin B | Orexin 2 receptor-selective agonist danavorexton improves narcolepsy phenotype in a mouse model and in human patients | 2022 | Narcolepsy mouse model plus single- and multiple-rising-dose intravenous studies in healthy adults and in patients with narcolepsy types 1 and 2 | Mixed evidence | PMID DOI |
| Ovagen | Tripeptides slow down aging process in renal cell culture | 2014 | In vitro, young and aged renal cell culture, with in silico DNA-binding modelling; Russian language | Preclinical only | PMID |
| Ovagen | Effects of short peptides on lymphocyte chromatin in senile subjects | 2004 | Ex vivo lymphocyte chromatin analysis from elderly donors | Preclinical only | PMID DOI |
| Oxytocin | Prophylactic oxytocin for the third stage of labour to prevent postpartum haemorrhage | 2019 | Cochrane systematic review and meta-analysis; 24 trials identified, 23 contributing data on 10,018 women | High-quality evidence | PMID DOI |
| Oxytocin | Intranasal Oxytocin in Children and Adolescents with Autism Spectrum Disorder | 2021 | 24-week randomised, double-blind, placebo-controlled phase 2 trial (SOARS-B); 290 children and adolescents aged 3-17 randomised, 250 completed; target dose 48 IU daily | High-quality evidence | PMID DOI Trial |
| Oxytocin | Effect of intranasal oxytocin on the core social symptoms of autism spectrum disorder: a randomized clinical trial | 2020 | Multicentre randomised, double-blind, parallel-group, placebo-controlled trial in Japan; 106 adults aged 18-48 with autism spectrum disorder, 103 analysed; 48 IU daily for six weeks | High-quality evidence | PMID DOI |
| Oxytocin | Intranasal Oxytocin: Myths and Delusions | 2016 | Critical narrative review of the pharmacological basis of intranasal oxytocin research - not primary data | Limited evidence | PMID DOI |
| P021 | Neurotrophic peptides incorporating adamantane improve learning and memory, promote neurogenesis and synaptic plasticity in mice | 2010 | Adult C57Bl/6 mice, peripheral administration, behavioural testing with neurogenesis readouts | Preclinical only | PMID DOI |
| P021 | Disease modifying effect of chronic oral treatment with a neurotrophic peptidergic compound in a triple transgenic mouse model of Alzheimer's disease | 2014 | Chronic oral treatment in 3xTg-AD triple transgenic mice | Preclinical only | PMID DOI |
| P021 | Rescue of cognitive-aging by administration of a neurogenic and/or neurotrophic compound | 2014 | Aged rodent model of cognitive ageing | Preclinical only | PMID DOI |
| P021 | Elevated Tau Level in Aged Rat Cerebrospinal Fluid Reduced by Treatment with a Neurotrophic Compound | 2015 | Aged rats with CSF tau measurement | Preclinical only | PMID DOI |
| P021 | Prevention of dendritic and synaptic deficits and cognitive impairment with a neurotrophic compound | 2017 | Transgenic mouse model, prevention paradigm | Preclinical only | PMID DOI |
| P021 | Early neurotrophic pharmacotherapy rescues developmental delay and Alzheimer's-like memory deficits in the Ts65Dn mouse model of Down syndrome | 2017 | Ts65Dn mouse model of Down syndrome, early treatment paradigm | Preclinical only | PMID DOI |
| P021 | Prenatal to early postnatal neurotrophic treatment prevents Alzheimer-like behavior and pathology in mice | 2020 | Transgenic mouse model with prenatal to early postnatal dosing | Preclinical only | PMID DOI |
| P021 | Neurotrophic factor small-molecule mimetics mediated neuroregeneration and synaptic repair: emerging therapeutic modality for Alzheimer's disease | 2016 | Review of neurotrophic factor small-molecule mimetics | Preclinical only | PMID DOI |
| palmitoyl hexapeptide-12 | Elastin binds to a multifunctional 67-kilodalton peripheral membrane protein | 1989 | Biochemical characterisation of receptor binding | PMID | |
| palmitoyl hexapeptide-12 | Peptide sequences selected by BA4, a tropoelastin-specific monoclonal antibody, are ligands for the 67-kilodalton bovine elastin receptor | 1993 | Peptide selection and receptor binding assay | PMID | |
| palmitoyl hexapeptide-12 | Conformational dependence of collagenase (matrix metalloproteinase-1) up-regulation by elastin peptides in cultured fibroblasts | 2001 | In vitro, cultured human fibroblasts | PMID | |
| palmitoyl hexapeptide-12 | Interaction between the elastin peptide VGVAPG and human elastin binding protein | 2013 | Binding and structural analysis | PMID | |
| palmitoyl hexapeptide-12 | The elastin peptide (VGVAPG)3 induces the 3D reorganisation of PML-NBs and SC35 speckles architecture, and accelerates proliferation of fibroblasts and melanoma cells | 2015 | In vitro, human fibroblasts and melanoma cells | Preclinical only | PMID |
| palmitoyl hexapeptide-12 | Noninvasive Monitoring of Palmitoyl Hexapeptide-12 in Human Skin Layers: Mechanical Interaction with Skin Components and Its Potential Skincare Benefits | 2025 | Label-free analytical study (orbital trapping secondary ion mass spectrometry, stimulated Raman scattering, high-throughput mechanical characterisation) on full-thickness human skin, plus in vitro tests and ex vivo histology | Preclinical only | PMID DOI |
| Palmitoyl pentapeptide-4 | A pentapeptide from type I procollagen promotes extracellular matrix production | 1993 | In vitro; dissection of the type I collagen C-terminal propeptide subfragment (residues 197-241) in subconfluent fibroblasts and other mesenchymal cells | Preclinical only | PMID |
| Palmitoyl pentapeptide-4 | Topical palmitoyl pentapeptide provides improvement in photoaged human facial skin | 2005 | Double-blind, placebo-controlled, split-face, left-right randomised; n=93 Caucasian women aged 35-55; 12 weeks; moisturiser containing 3 ppm pal-KTTKS versus the same moisturiser alone | Mixed evidence | PMID DOI |
| Palmitoyl pentapeptide-4 | Double-blind, Randomized Trial on the Effectiveness of Acetylhexapeptide-3 Cream and Palmitoyl Pentapeptide-4 Cream for Crow's Feet | 2023 | Double-blind randomised trial, three parallel arms of 7 subjects each (n=21 Indonesian women aged 26-55), 8 weeks, twice-daily periorbital application | Limited evidence | PMID |
| palmitoyl tetrapeptide-7 | Rigin, another phagocytosis-stimulating tetrapeptide isolated from human IgG. Confirmations of a hypothesis | 1981 | Peptide isolation and in vitro phagocytosis assay | PMID | |
| palmitoyl tetrapeptide-7 | Characterization of a novel type VII beta-turn conformation for a bio-active tetrapeptide rigin. A synergy between theoretical and experimental results | 2000 | NMR and computational conformational analysis | PMID | |
| palmitoyl tetrapeptide-7 | Immunomodulatory potential of hydrophobic analogs of Rigin and their role in providing protection against Plasmodium berghei infection in mice | 2001 | In vivo murine immunomodulation and infection challenge | Preclinical only | PMID |
| palmitoyl tetrapeptide-7 | Folded conformation of an immunostimulating tetrapeptide rigin: high temperature molecular dynamics simulation study | 2002 | Molecular dynamics simulation | PMID | |
| palmitoyl tripeptide-1 | Structure of the Glycyl-L-histidyl-L-lysine--copper(II) complex in solution | 1982 | Physicochemical study (EPR, ENDOR, spectroscopy) of copper co-ordination | PMID DOI | |
| palmitoyl tripeptide-1 | Stimulation of sulfated glycosaminoglycan synthesis by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+ | 1992 | In vitro, cultured fibroblasts | Preclinical only | PMID DOI |
| palmitoyl tripeptide-1 | The tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+ stimulates matrix metalloproteinase-2 expression by fibroblast cultures | 2000 | In vitro, human dermal fibroblasts | Preclinical only | PMID |
| palmitoyl tripeptide-1 | Collagen stimulating effect of peptide amphiphile C16-KTTKS on human fibroblasts | 2013 | In vitro biophysics plus fibroblast culture | Preclinical only | PMID |
| palmitoyl tripeptide-1 | Targeting Circadian Rhythm for the Regulation of Skin Collagen Metabolism | 2026 | Circadian-synchronised fibroblast model and 8-week murine topical study, plus a 30-participant clinical study of a timed two-ingredient regimen | PMID DOI | |
| palmitoyl tripeptide-1 | Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data | 2018 | Narrative review | PMID | |
| palmitoyl tripeptide-1 | Topically applied GHK as an anti-wrinkle peptide: Advantages, problems and prospective | 2025 | Narrative review of topical GHK formulation and delivery | Preclinical only | PMID DOI |
| palmitoyl tripeptide-1 | Biological activities of selected peptides: skin penetration ability of copper complexes with peptides | 2008 | In vitro skin penetration comparison of peptide-copper complexes | Preclinical only | PMID |
| palmitoyl tripeptide-1 | Human skin retention and penetration of a copper tripeptide in vitro as function of skin layer towards anti-inflammatory therapy | 2010 | In vitro human skin, penetration by layer | Preclinical only | PMID DOI |
| palmitoyl tripeptide-1 | Liposomes as Carriers of GHK-Cu Tripeptide for Cosmetic Application | 2023 | Formulation and in vitro characterisation of liposomal GHK-Cu | Preclinical only | PMID DOI |
| palmitoyl tripeptide-5 | Efficacy of bioactive peptides loaded on hyaluronic acid microneedle patches: A monocentric clinical study | 2020 | 12-week uncontrolled monocentric clinical study of hyaluronic acid microneedle patches containing five actives including palmitoyl tripeptide-5 | PMID DOI | |
| palmitoyl tripeptide-5 | Usage of Synthetic Peptides in Cosmetics for Sensitive Skin | 2021 | Narrative review of cosmetic peptide ingredients | PMID | |
| palmitoyl tripeptide-5 | The type 1 repeats of thrombospondin 1 activate latent transforming growth factor-beta | 1994 | In vitro biochemistry and cell culture | PMID | |
| palmitoyl tripeptide-5 | Regulation of transforming growth factor-beta activation by discrete sequences of thrombospondin 1 | 1995 | Peptide mapping and activation assays | PMID | |
| palmitoyl tripeptide-5 | The activation sequence of thrombospondin-1 interacts with the latency-associated peptide to regulate activation of latent transforming growth factor-beta | 1999 | Direct binding and functional activation studies | PMID | |
| palmitoyl tripeptide-5 | Expression of the type-1 repeats of thrombospondin-1 inhibits tumor growth through activation of transforming growth factor-beta | 2004 | In vivo murine tumour model | Preclinical only | PMID |
| Pancragen | Prospects of using pancragen for correction of metabolic disorders in elderly people | 2011 | Small non-randomised human study, 30 healthy older people and 33 older patients with type 2 diabetes, with an untreated diabetic comparison group | Limited evidence | PMID DOI |
| Pancragen | Correction of impaired glucose tolerance using tetrapeptide (Pancragen) in old female rhesus monkeys | 2015 | Non-human primate, aged female rhesus monkeys with impaired glucose tolerance; Russian language | Preclinical only | PMID |
| Pancragen | Impact of tetrapeptide pancragen on endocrine function of the pancreas in old monkeys | 2014 | Non-human primate, aged monkeys; Russian language | Preclinical only | PMID |
| Pancragen | Effect of pancragen on blood glucose level, capillary permeability and adhesion in rats with experimental diabetes mellitus | 2007 | Rat model of experimental diabetes mellitus | Preclinical only | PMID DOI |
| Pancragen | Effects of pancragen on the differentiation of pancreatic cells during their ageing | 2013 | In vitro, ageing pancreatic cell culture | Preclinical only | PMID DOI |
| Pancragen | Feasibility of Transport of 26 Biologically Active Ultrashort Peptides via LAT and PEPT Family Transporters | 2023 | In silico molecular modelling and docking against LAT1, LAT2 and PEPT1 transporters | Preclinical only | PMID DOI |
| Parathyroid hormone (1-84) | Effect of recombinant human parathyroid hormone (1-84) on vertebral fracture and bone mineral density in postmenopausal women with osteoporosis: a randomized trial | 2007 | Randomised, double-blind, placebo-controlled phase 3 trial; n=2,532 postmenopausal women with osteoporosis; 18 months. Published as 146(5):326-39. | PMID DOI | |
| Parathyroid hormone (1-84) | Efficacy and safety of recombinant human parathyroid hormone (1-84) in hypoparathyroidism (REPLACE): a double-blind, placebo-controlled, randomised, phase 3 study | 2013 | Randomised, double-blind, placebo-controlled phase 3 trial; 134 adults with chronic hypoparathyroidism across 33 centres; 24 weeks. Published as 1(4):275-283. | PMID DOI | |
| Parathyroid hormone (1-84) | The effects of parathyroid hormone and alendronate alone or in combination in postmenopausal osteoporosis | 2003 | Randomised trial of PTH(1-84), alendronate, or both; n=238 postmenopausal women; 12 months. Published as 349(13):1207-15. | PMID DOI | |
| Parathyroid hormone (1-84) | Long-term safety and efficacy of recombinant human parathyroid hormone (1-84) in adults with chronic hypoparathyroidism | 2023 | Multicentre open-label extension study (RACE), up to 8 years of continuous treatment. Published as 7(5):bvad043. | PMID DOI | |
| Pasireotide | A 12-month phase 3 study of pasireotide in Cushing's disease | 2012 | Randomised, double-blind phase 3 trial in 162 adults with Cushing's disease and urinary free cortisol at least 1.5 times the upper limit of normal; subcutaneous pasireotide 600 micrograms (n=82) or 900 micrograms (n=80) twice daily, with open-label continuation through month 12 | PMID DOI Trial | |
| Pasireotide | Pasireotide versus octreotide in acromegaly: a head-to-head superiority study | 2014 | Prospective, randomised, double-blind superiority trial at 84 sites in 27 countries in 358 medically naive patients with acromegaly; pasireotide LAR 40 mg (n=176) versus octreotide LAR 20 mg (n=182) every 28 days for 12 months, with optional titration at months 3 and 7 | PMID DOI | |
| Pasireotide | Pasireotide versus continued treatment with octreotide or lanreotide in patients with inadequately controlled acromegaly (PAOLA): a randomised, phase 3 trial | 2014 | Multicentre randomised phase 3 trial in 198 patients with acromegaly inadequately controlled after at least 6 months of octreotide LAR 30 mg or lanreotide 120 mg; pasireotide LAR 40 mg (n=65) or 60 mg (n=65) every 28 days for 24 weeks versus continued first-generation analogue (n=68). Patients and investigators were not masked to study drug assignment but were masked to pasireotide dose | PMID DOI Trial | |
| PE 22-28 | Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity | 2017 | Structure-activity study of truncated spadin analogues: patch-clamp electrophysiology on hTREK-1/HEK cells plus mouse forced swimming and novelty-suppressed feeding paradigms | Preclinical only | PMID DOI |
| PE 22-28 | Spadin, a sortilin-derived peptide, targeting rodent TREK-1 channels: a new concept in the antidepressant drug design | 2010 | Identification and characterisation of spadin with electrophysiology and mouse behavioural models | Preclinical only | PMID DOI |
| PE 22-28 | First evidence of protective effects on stroke recovery and post-stroke depression induced by sortilin-derived peptides | 2019 | Mouse focal ischaemia and post-stroke depression model, with electrophysiology; a single low intraperitoneal dose of 0.03 µg/kg daily for 7 days post-ischaemia, then 3 µg/kg for 4 days a week thereafter | Preclinical only | PMID DOI |
| PE 22-28 | Spadin as a new antidepressant: absence of TREK-1-related side effects | 2012 | Mouse studies examining side effects anticipated from TREK-1 blockade | Preclinical only | PMID DOI |
| PE 22-28 | In vitro and in vivo regulation of synaptogenesis by the novel antidepressant spadin | 2015 | In vitro neuronal culture and in vivo mouse synaptogenesis study | Preclinical only | PMID DOI |
| PE 22-28 | Fighting against depression with TREK-1 blockers: Past and future. A focus on spadin | 2019 | Review of TREK-1 blockade as an antidepressant strategy | Preclinical only | PMID DOI |
| PE 22-28 | The Involvement of Sortilin/NTSR3 in Depression as the Progenitor of Spadin and Its Role in the Membrane Expression of TREK-1 | 2018 | Review of sortilin biology and its relationship to TREK-1 membrane expression | Preclinical only | PMID DOI |
| PEG-MGF (pegylated mechano growth factor) | Minireview: Mechano-growth factor: a putative product of IGF-I gene expression involved in tissue repair and regeneration | 2010 | Critical review of the MGF literature | Preclinical only | PMID DOI |
| PEG-MGF (pegylated mechano growth factor) | Insulin-like growth factor-I E-peptide activity is dependent on the IGF-I receptor | 2012 | Receptor-dependence experiments in cultured muscle cells | Preclinical only | PMID DOI |
| PEG-MGF (pegylated mechano growth factor) | Mass spectrometric characterization of a biotechnologically produced full-length mechano growth factor (MGF) relevant for doping controls | 2014 | Analytical characterisation by mass spectrometry of commercially produced MGF | Limited evidence | PMID DOI |
| PEG-MGF (pegylated mechano growth factor) | Detection and in vitro metabolism of the confiscated peptides BPC 157 and MGF R23H | 2017 | Analytical characterisation and in vitro metabolic stability of black-market peptides | Limited evidence | PMID DOI |
| PEG-MGF (pegylated mechano growth factor) | The emerging landscape of performance-enhancing peptides modulating GH-IGF1 axis: bridging the gap between clinical evidence and patient self-administration | 2026 | Narrative review of growth hormone and IGF-1 axis peptides used outside clinical supervision | Limited evidence | PMID DOI |
| pentapeptide-18 | Enkephalin reduces quantal content at the frog neuromuscular junction | 1983 | Electrophysiology in isolated nerve-muscle preparation | PMID | |
| pentapeptide-18 | Leu-enkephalin effects at the mouse neuromuscular junction | 1990 | Ex vivo mouse neuromuscular preparation | Preclinical only | PMID |
| pentapeptide-18 | D-tyrosine adds an anti-melanogenic effect to cosmetic peptides | 2020 | In vitro, MNT-1 melanoma cells, primary human melanocytes and a 3D human skin model | Preclinical only | PMID DOI |
| pentapeptide-18 | Pentapeptide-18 as an anti-aging candidate: Spectroscopic characterization and molecular interaction analysis | 2026 | FTIR, ATR-FTIR and Raman spectroscopy with density functional theory, molecular docking, molecular dynamics and ADMET prediction | Preclinical only | PMID DOI |
| pentapeptide-18 | Deletion of delta-opioid receptor in mice alters skin differentiation and delays wound healing | 2006 | Knockout mouse model | Preclinical only | PMID |
| pentapeptide-18 | Peripheral Opioids | 2014 | Narrative review | PMID | |
| Peptide YY (PYY 3-36) | Gut hormone PYY(3-36) physiologically inhibits food intake | 2002 | Rodent studies plus randomised, blinded crossover infusion in healthy human volunteers | PMID | |
| Peptide YY (PYY 3-36) | Inhibition of food intake in obese subjects by peptide YY3-36 | 2003 | Randomised, double-blind, placebo-controlled crossover infusion study in obese and lean subjects | PMID | |
| Peptide YY (PYY 3-36) | Physiology: does gut hormone PYY3-36 decrease food intake in rodents? | 2004 | Large multi-laboratory rodent replication attempt | PMID | |
| Peptide YY (PYY 3-36) | Efficacy and safety of intranasal peptide YY3-36 for weight reduction in obese adults | 2007 | Randomised, double-blind, placebo-controlled trial with 2-week placebo run-in and 12 weeks of preprandial intranasal dosing in obese adults | PMID | |
| Pinealon | Pinealon increases cell viability by suppression of free radical levels and activating proliferative processes | 2011 | In vitro, cerebellar granule cells, neutrophils and PC12 cells under receptor-dependent and receptor-independent oxidative stress | Preclinical only | PMID DOI |
| Pinealon | Pinealon protects the rat offspring from prenatal hyperhomocysteinemia | 2012 | Rodent, prenatal hyperhomocysteinaemia model | Preclinical only | PMID |
| Pinealon | EDR Peptide: Possible Mechanism of Gene Expression and Protein Synthesis Regulation Involved in the Pathogenesis of Alzheimer's Disease | 2020 | Review with in vitro gene expression analysis | Preclinical only | PMID DOI |
| Pinealon | Penetration of short fluorescence-labeled peptides into the nucleus in HeLa cells and in vitro specific interaction of the peptides with deoxyribooligonucleotides and DNA | 2011 | In vitro, fluorescence microscopy and oligonucleotide fluorescence-quenching assays | Preclinical only | PMID DOI |
| Pinealon | Feasibility of Transport of 26 Biologically Active Ultrashort Peptides via LAT and PEPT Family Transporters | 2023 | In silico molecular modelling and docking of 26 ultrashort peptides against LAT1, LAT2 and PEPT1 transporters, benchmarked against all 8400 possible di- and tripeptides | Preclinical only | PMID DOI |
| Pinealon | Neuroprotective effects of peptide bioregulators in people of various age | 2013 | Small uncontrolled human observation, Russian language | Limited evidence | PMID |
| Plecanatide | A randomized phase III clinical trial of plecanatide, a uroguanylin analog, in patients with chronic idiopathic constipation | 2017 | Phase 3 multicentre randomised, double-blind, placebo-controlled trial, 1,394 patients, 12 weeks | PMID | |
| Plecanatide | Randomized clinical trial: efficacy and safety of plecanatide in the treatment of chronic idiopathic constipation | 2017 | Phase 3 randomised, double-blind, placebo-controlled trial, 1,337 patients (3 mg n=443, 6 mg n=449, placebo n=445), 12 weeks | PMID | |
| Plecanatide | Efficacy, safety, and tolerability of plecanatide in patients with irritable bowel syndrome with constipation: results of two phase 3 randomized clinical trials | 2018 | Two identical phase 3 randomised, double-blind, placebo-controlled trials, 2,189 randomised (1,879 completed), 12 weeks, Rome III criteria | PMID | |
| PNC-27 | Anticancer peptide PNC-27 adopts an HDM-2-binding conformation and kills cancer cells by binding to HDM-2 in their membranes | 2010 | Structural comparison plus cell-based colocalisation and transfection experiments in cancer and untransformed cell lines | Preclinical only | PMID DOI |
| PNC-27 | PNC-28, a p53-derived peptide that is cytotoxic to cancer cells, blocks pancreatic cancer cell growth in vivo | 2006 | In vitro cytotoxicity plus in vivo xenograft model of pancreatic cancer | Preclinical only | PMID DOI |
| PNC-27 | The penetratin sequence in the anticancer PNC-28 peptide causes tumor cell necrosis rather than apoptosis of human pancreatic cancer cells | 2008 | In vitro mechanistic study in human pancreatic cancer cell lines | Preclinical only | PMID DOI |
| PNC-27 | The anti-cancer peptide, PNC-27, induces tumor cell necrosis of a poorly differentiated non-solid tissue human leukemia cell line that depends on expression of HDM-2 in the plasma membrane of these cells | 2014 | In vitro study in p53-null K562 human leukaemia cells with murine leukocytes as non-cancer control; LDH release for necrosis, caspase 3/7 for apoptosis, antibody colocalisation microscopy | Preclinical only | PMID |
| PNC-27 | PNC-27, a Chimeric p53-Penetratin Peptide Binds to HDM-2 in a p53 Peptide-like Structure, Induces Selective Membrane-Pore Formation and Leads to Cancer Cell Lysis | 2022 | Conformational energy calculations plus immuno-scanning electron microscopy of PNC-27-treated cancer cells using 6 nm gold anti-PNC-27 and 15 nm gold anti-HDM-2 antibodies, with untransformed fibroblast controls | Preclinical only | PMID DOI |
| PNC-27 | Anti-Cancer Peptide PNC-27 Kills Cancer Cells by Unique Interactions with Plasma Membrane-Bound hdm-2 and with Mitochondrial Membranes Causing Mitochondrial Disruption | 2024 | In vitro study in MIA-PaCa-2 human pancreatic carcinoma cells using an antibody-blocking experiment, mitotracker and lysotracker dyes, and immuno-electron microscopy | Preclinical only | PMID |
| Polymyxin B | Polymyxin B versus colistin: an update | 2015 | Comparative narrative review of pharmacology, pharmacokinetics and clinical outcome data | PMID DOI | |
| Polymyxin B | Uptake of polymyxin B into renal cells | 2014 | Cell-based mechanistic study of renal tubular transport (Antimicrob Agents Chemother 58(7):4200-2) | PMID DOI | |
| Polymyxin B | Potent activity of polymyxin B is associated with long-lived super-stoichiometric accumulation mediated by weak-affinity binding to lipid A | 2024 | Single-molecule biophysical and microbiological mechanistic study | DOI | |
| Polymyxin B | Structure-activity relationships of polymyxin antibiotics | 2010 | Systematic structure-activity review of the polymyxin scaffold (J Med Chem 53(5):1898-1916) | PMID DOI | |
| Polymyxin B | Effect of Targeted Polymyxin B Hemoperfusion on 28-Day Mortality in Patients With Septic Shock and Elevated Endotoxin Level: The EUPHRATES Randomized Clinical Trial | 2018 | Multicentre randomised sham-controlled trial of polymyxin B-immobilised haemoperfusion in septic shock with elevated endotoxin activity; 450 participants (JAMA 320(14):1455-1463) | PMID DOI Trial | |
| Pramlintide | A randomized study and open-label extension evaluating the long-term efficacy of pramlintide as an adjunct to insulin therapy in type 1 diabetes | 2002 | 52-week randomised, double-blind, placebo-controlled multicentre trial with a one-year open-label extension; 480 adults with type 1 diabetes randomised, 342 completed 52 weeks, 236 entered the extension | PMID DOI | |
| Pramlintide | Pramlintide as an adjunct to insulin therapy improves long-term glycemic and weight control in patients with type 2 diabetes: a 1-year randomized controlled trial | 2003 | 52-week randomised, double-blind, placebo-controlled trial, 656 insulin-treated adults with type 2 diabetes | PMID DOI | |
| Pramlintide | Amylin replacement with pramlintide as an adjunct to insulin therapy improves long-term glycaemic and weight control in Type 1 diabetes mellitus: a 1-year, randomized controlled trial | 2004 | 52-week randomised, double-blind, placebo-controlled, parallel-group multicentre trial, 651 adults with type 1 diabetes | PMID DOI | |
| Pramlintide | Pramlintide improved glycemic control and reduced weight in patients with type 2 diabetes using basal insulin | 2007 | 16-week randomised, double-blind, placebo-controlled trial, 212 adults with type 2 diabetes using insulin glargine | PMID DOI | |
| Prostamax | Deheterochromatinization of the chromatin in old age induced by oligopeptide bioregulator (Lys-Glu-Asp-Pro) | 2012 | Ex vivo cytogenetic analysis of cells from donors aged 75-86 exposed to Prostamax; Russian language | Preclinical only | PMID |
| Prostamax | The influence of the peptide bioregulator prostamax on heterochromatin of human lymphocytes in situ | 2004 | Differential scanning microcalorimetry of human lymphocyte chromatin in situ; Russian language | Preclinical only | PMID |
| Prostamax | Microcalorimetric study of human blood lymphocytes culture at presence of copper, cadmium and prostamax | 2009 | Microcalorimetry of lymphocyte cultures from ageing donors with Prostamax and copper or cadmium ions | Preclinical only | PMID |
| Prostamax | Feasibility of Transport of 26 Biologically Active Ultrashort Peptides via LAT and PEPT Family Transporters | 2023 | In silico molecular modelling and docking against LAT1, LAT2 and PEPT1 transporters | Preclinical only | PMID DOI |
| Prostamax | Effects of short peptides on lymphocyte chromatin in senile subjects | 2004 | Ex vivo lymphocyte chromatin analysis from elderly donors | Preclinical only | PMID DOI |
| Protirelin | Amyotrophic lateral sclerosis: effects of acute intravenous and chronic subcutaneous administration of thyrotropin-releasing hormone in controlled trials | 1986 | Double-blind crossover controlled trials of both acute intravenous and chronic subcutaneous TRH administration in patients with amyotrophic lateral sclerosis | PMID DOI | |
| Protirelin | Low doses of TRH in amyotrophic lateral sclerosis and in other neurological diseases | 1991 | Uncontrolled study of chronic low-dose TRH therapy in 30 subjects: 23 with amyotrophic lateral sclerosis, 4 with Charcot-Marie-Tooth atrophy, 2 with progressive spinal muscular atrophy and 1 with radiation myelopathy, assessed on the Norris scale | PMID DOI | |
| Protirelin | Approved product labelling: protirelin (thyrotropin releasing hormone) injection | 2009 | Regulator-approved labelling summarising pharmacology, diagnostic performance and safety of intravenous protirelin | none | |
| PTD-DBM | The Dishevelled-binding protein CXXC5 negatively regulates cutaneous wound healing | 2015 | CXXC5-knockout mice, mouse cutaneous wound models, human wound tissue and cell-based interaction studies | Preclinical only | PMID DOI |
| PTD-DBM | Targeting of CXXC5 by a Competing Peptide Stimulates Hair Regrowth and Wound-Induced Hair Neogenesis | 2017 | CXXC5-knockout mice, mouse hair regrowth and wound-induced neogenesis models, human hair follicle dermal papilla cell culture, human balding scalp tissue | Preclinical only | PMID DOI |
| PTD-DBM | CXXC5 Mediates DHT-Induced Androgenetic Alopecia via PGD2 | 2023 | Cell and mouse models of dihydrotestosterone-driven follicular changes | Preclinical only | PMID DOI |
| PTD-DBM | Adhesive Hydrogel Patch-Mediated Combination Drug Therapy Induces Regenerative Wound Healing through Reconstruction of Regenerative Microenvironment | 2023 | Mouse wound model with hydrogel patch delivery of combination therapy | Preclinical only | PMID DOI |
| Retatrutide | Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial | 2023 | Randomised, double-blind, placebo-controlled phase 2 trial, n=338, 48 weeks | Mixed evidence | PMID DOI Trial |
| Retatrutide | Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial conducted in the USA | 2023 | Randomised, double-blind, placebo- and active-controlled (dulaglutide 1.5 mg) phase 2 trial, n=281, 36 weeks | Mixed evidence | PMID DOI |
| Retatrutide | TRIUMPH-1 phase 3 trial of retatrutide in obesity (sponsor topline announcement) | 2026 | Randomised, double-blind, placebo-controlled phase 3 trial, n=2,339 randomised 1:1:1:1 to 4 mg, 9 mg, 12 mg or placebo, 80 weeks with an extension to 104 weeks | Limited evidence | none |
| romidepsin | Phase II multi-institutional trial of the histone deacetylase inhibitor romidepsin as monotherapy for patients with cutaneous T-cell lymphoma | 2009 | Open-label single-arm phase 2, 71 patients with cutaneous T-cell lymphoma | PMID DOI | |
| romidepsin | Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma | 2010 | Open-label single-arm international pivotal phase 2, 96 patients with refractory cutaneous T-cell lymphoma | PMID DOI | |
| romidepsin | Results from a pivotal, open-label, phase II study of romidepsin in relapsed or refractory peripheral T-cell lymphoma after prior systemic therapy | 2012 | Open-label single-arm pivotal phase 2, 130 patients with relapsed/refractory peripheral T-cell lymphoma | PMID DOI | |
| romidepsin | Romidepsin plus CHOP versus CHOP in patients with previously untreated peripheral T-cell lymphoma: results of the Ro-CHOP phase III study (conducted by LYSA) | 2022 | Randomised open-label phase 3, 421 patients with previously untreated peripheral T-cell lymphoma | PMID DOI | |
| romidepsin | Romidepsin plus cyclophosphamide, doxorubicin, vincristine, and prednisone versus cyclophosphamide, doxorubicin, vincristine, and prednisone in patients with previously untreated peripheral T-cell lymphoma: final analysis of the Ro-CHOP trial | 2024 | Final long-term analysis of the Ro-CHOP randomised phase 3 trial | PMID DOI | |
| Salmon calcitonin | A randomized trial of nasal spray salmon calcitonin in postmenopausal women with established osteoporosis: the Prevent Recurrence of Osteoporotic Fractures study | 2000 | Randomised, double-blind, placebo-controlled trial; n=1,255 postmenopausal women; 5 years; three nasal doses. Published as 109(4):267-76. | PMID DOI | |
| Salmon calcitonin | Article 31 referral: calcitonin-containing medicines, CHMP outcome | 2012 | Regulatory benefit-risk review pooling randomised controlled trials, post-marketing safety data and non-clinical carcinogenicity evidence across all calcitonin formulations. Procedure initiated 2010; CHMP opinion 19 July 2012; European Commission decision 13 February 2013. | none | |
| Salmon calcitonin | Calcitonin for treating acute and chronic pain of recent and remote osteoporotic vertebral compression fractures: a systematic review and meta-analysis | 2012 | Systematic review and meta-analysis of randomised controlled trials of calcitonin for vertebral fracture pain. Published as 23(1):17-38. | PMID DOI | |
| Salmon calcitonin | Treatment of symptomatic knee osteoarthritis with oral salmon calcitonin: results from two phase 3 trials | 2015 | Two randomised, double-blind, placebo-controlled phase 3 trials of oral salmon calcitonin in knee osteoarthritis; 24 months. Published as 23(4):532-43. | PMID DOI | |
| Secretin | Lack of benefit of a single dose of synthetic human secretin in the treatment of autism and pervasive developmental disorder | 1999 | Double-blind, placebo-controlled randomised trial of a single intravenous dose of synthetic human secretin versus placebo in 60 children aged 3 to 14 years with autism or pervasive developmental disorder; 56 children (28 per group) completed the four-week follow-up | PMID DOI | |
| Secretin | Intravenous secretin for autism spectrum disorders (ASD) | 2012 | Systematic review of randomised placebo-controlled trials of single or multiple intravenous secretin doses in autism spectrum disorders; 16 studies met the inclusion criteria, with usable outcome data available from 14 of them | PMID DOI | |
| Secretin | An endoscopic pancreatic function test with synthetic porcine secretin for the evaluation of chronic abdominal pain and suspected chronic pancreatitis | 2003 | Small prospective study of an endoscopic secretin-stimulated pancreatic function test in 18 patients across three groups: 5 with chronic abdominal pain without risk factors, 7 with pain plus risk factors for chronic pancreatitis, and 6 with advanced chronic pancreatitis | PMID DOI | |
| Secretin | Magnetic resonance cholangiopancreatography in the diagnosis of pancreas divisum: a systematic review and meta-analysis | 2014 | Systematic review and meta-analysis of 10 studies including 1,474 patients evaluating magnetic resonance cholangiopancreatography, with and without secretin enhancement, against reference standards for pancreas divisum | PMID DOI | |
| Selank | Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia | 2008 | Active-comparator clinical study, n=62 (Selank 30, medazepam 32), Hamilton, Zung and CGI psychometric scales plus serum enkephalin activity; no placebo arm; Russian-language | Limited evidence | PMID |
| Selank | A comparison of the anxiolytic effect and tolerability of selank and phenazepam in the treatment of anxiety disorders | 2014 | Comparative clinical study versus the benzodiazepine phenazepam in 60 patients with phobic-anxiety and somatoform disorders (ICD-10 F40.2-9, F41.1-9, F45.0-1); Russian-language | Limited evidence | PMID |
| Selank | The inhibitory effect of Selank on enkephalin-degrading enzymes as a possible mechanism of its anxiolytic activity | 2001 | Enzyme activity study | Preclinical only | PMID DOI |
| Selank | Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission | 2016 | Gene expression analysis in rat brain following Selank administration | Preclinical only | PMID DOI |
| Selank | Peptide Selank Enhances the Effect of Diazepam in Reducing Anxiety in Unpredictable Chronic Mild Stress Conditions in Rats | 2017 | Rat unpredictable chronic mild stress model | Preclinical only | PMID DOI |
| Selank | Selank, a Peptide Analog of Tuftsin, Attenuates Aversive Signs of Morphine Withdrawal in Rats | 2022 | Rat morphine withdrawal model | Preclinical only | PMID DOI |
| Selank | Effects of Selank on behavioral reactions and activities of plasma enkephalin-degrading enzymes in mice | 2002 | Mouse behavioural pharmacology with plasma enzyme assays | Preclinical only | PMID DOI |
| Semaglutide | Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes | 2016 | Randomised, double-blind, placebo-controlled cardiovascular outcome trial, n=3,297, median 2.1 years | High-quality evidence | PMID DOI |
| Semaglutide | Once-Weekly Semaglutide in Adults with Overweight or Obesity | 2021 | Randomised, double-blind, placebo-controlled phase 3 trial, n=1,961, 68 weeks | High-quality evidence | PMID DOI Trial |
| Semaglutide | Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes | 2023 | Randomised, double-blind, placebo-controlled cardiovascular outcome trial, n=17,604, mean follow-up approximately 40 months | High-quality evidence | PMID DOI Trial |
| Semaglutide | Effects of Semaglutide on Chronic Kidney Disease in Patients with Type 2 Diabetes | 2024 | Randomised, double-blind, placebo-controlled outcome trial, n=3,533 | High-quality evidence | PMID DOI |
| Semaglutide | Phase 3 Trial of Semaglutide in Metabolic Dysfunction-Associated Steatohepatitis | 2025 | Randomised, double-blind, placebo-controlled phase 3 trial; planned interim histology analysis of the first 800 of 1,197 randomised participants at 72 weeks | High-quality evidence | PMID DOI |
| Semaglutide | Oral semaglutide 50 mg taken once per day in adults with overweight or obesity (OASIS 1): a randomised, double-blind, placebo-controlled, phase 3 trial | 2023 | Randomised, double-blind, placebo-controlled phase 3 trial, n=709, 68 weeks | High-quality evidence | PMID DOI |
| Semax | Semax, an analogue of adrenocorticotropin (4-10), binds specifically and increases levels of brain-derived neurotrophic factor protein in rat basal forebrain | 2006 | In vitro radioligand binding and in vivo protein quantification, rat basal forebrain | Preclinical only | PMID DOI |
| Semax | The heptapeptide SEMAX stimulates BDNF expression in different areas of the rat brain in vivo | 2003 | In vivo rodent study of regional BDNF expression | Preclinical only | PMID DOI |
| Semax | Semax, an ACTH(4-10) analogue with nootropic properties, activates dopaminergic and serotoninergic brain systems in rodents | 2005 | Rodent neurochemistry, monoamine turnover | Preclinical only | PMID DOI |
| Semax | The peptide semax affects the expression of genes related to the immune and vascular systems in rat brain focal ischemia: genome-wide transcriptional analysis | 2014 | Genome-wide transcriptomic analysis, rat focal cerebral ischaemia model | Preclinical only | PMID DOI |
| Semax | Effectiveness of semax in acute period of hemispheric ischemic stroke (a clinical and electrophysiological study) | 1997 | Non-randomised controlled clinical and electrophysiological study: 30 patients given Semax added to standard intensive therapy versus a separate control group of 80 patients on conventional therapy alone; no placebo and no blinding described. Daily doses were 12 mg in moderate strokes and 18 mg in severe strokes, over 5- and 10-day courses. Russian-language report. | Limited evidence | PMID |
| Semax | Evaluation of therapeutic effect of new Russian drug semax in optic nerve disease | 2000 | Open clinical study in vascular, toxic-allergic and inflammatory optic nerve disease and partial optic atrophy; patients divided into three groups (intranasal drops, endonasal electrophoresis, and control) with Semax given alongside standard neurotrophic and anti-inflammatory therapy. Sample size not stated in the abstract. Russian-language report. | Limited evidence | PMID |
| Semax | Kinetics of Semax penetration into the brain and blood of rats after its intranasal administration | 2006 | Pharmacokinetic study of labelled Semax in rats after intranasal administration | Preclinical only | PMID DOI |
| Semax | N-terminal degradation of ACTH(4-10) and its synthetic analog semax by the rat blood enzymes | 1991 | In vitro enzymatic degradation study in rat blood | Preclinical only | PMID DOI |
| Serelaxin | Relaxin for the treatment of patients with acute heart failure (Pre-RELAX-AHF): a multicentre, randomised, placebo-controlled, parallel-group, dose-finding phase IIb study | 2009 | Multicentre randomised placebo-controlled dose-finding phase 2b trial in acute heart failure | PMID | |
| Serelaxin | Serelaxin, recombinant human relaxin-2, for treatment of acute heart failure (RELAX-AHF): a randomised, placebo-controlled trial | 2013 | Randomised double-blind placebo-controlled phase 3 trial, 1161 patients hospitalised with acute heart failure, 48-hour infusion | PMID | |
| Serelaxin | Effects of Serelaxin in Patients with Acute Heart Failure | 2019 | Randomised double-blind placebo-controlled phase 3 trial (RELAX-AHF-2), 6545 patients, 48-hour serelaxin infusion versus placebo | PMID | |
| Serelaxin | Effects of serelaxin in patients admitted for acute heart failure: a meta-analysis | 2020 | Meta-analysis pooling randomised serelaxin trials in acute heart failure | PMID | |
| Sermorelin | Once daily subcutaneous growth hormone-releasing hormone therapy accelerates growth in growth hormone-deficient children during the first year of therapy | 1996 | Multicentre, open-label, uncontrolled study; 110 previously untreated prepubertal children with growth hormone deficiency enrolled, 86 eligible for analysis; GHRH(1-29) 30 micrograms/kg/day subcutaneously at bedtime for up to 12 months | Limited evidence | PMID DOI |
| Sermorelin | Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency | 1999 | Narrative review of diagnostic and therapeutic clinical data; not a primary study | Limited evidence | PMID DOI |
| Sermorelin | Effects of single nightly injections of growth hormone-releasing hormone (GHRH 1-29) in healthy elderly men | 1997 | Open-label, uncontrolled study; 11 healthy non-obese men aged 64-76 with low baseline IGF-1; GHRH(1-29) 2 mg nightly by subcutaneous self-injection for 6 weeks | Limited evidence | PMID DOI |
| Sermorelin | Determination That GEREF (Sermorelin Acetate) Injection, 0.5 Milligrams Base/Vial and 1.0 Milligrams Base/Vial, and GEREF (Sermorelin Acetate) Injection, 0.05 Milligrams Base/Amp, Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness | 2013 | Regulatory determination published 4 March 2013; not a clinical study | Limited evidence | none |
| Setmelanotide | MC4R agonism promotes durable weight loss in patients with leptin receptor deficiency | 2018 | Small open-label proof-of-concept study in patients with leptin receptor deficiency | PMID | |
| Setmelanotide | Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials | 2020 | Two parallel single-arm, open-label, multicentre phase 3 trials across ten hospitals in seven countries; 10 participants with POMC deficiency and 11 with LEPR deficiency, aged 6 years and over. No control group. | PMID | |
| Setmelanotide | Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alström syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period | 2022 | Multicentre randomised double-blind placebo-controlled phase 3 trial with a 14-week blinded period followed by a 52-week open-label period, across 12 sites in five countries; 38 patients randomised 19:19, comprising 16 with Bardet-Biedl syndrome and 3 with Alström syndrome per group | PMID | |
| Somatostatin | Hypothalamic polypeptide that inhibits the secretion of immunoreactive pituitary growth hormone | 1973 | Isolation, sequencing and synthetic replication of a hypothalamic peptide from ovine tissue, with bioassay in pituitary cell culture and in living rats | PMID DOI | |
| Somatostatin | Somatostatin analogues for acute bleeding oesophageal varices | 2008 | Systematic review and meta-analysis of 21 randomised trials in 2,588 patients comparing somatostatin or its analogues with placebo or no treatment in acute or recent bleeding from oesophageal varices | PMID DOI | |
| Somatostatin | Vasoactive Agents for the Management of Acute Variceal Bleeding: A Systematic Review and Meta-analysis | 2021 | Systematic review and meta-analysis of 21 randomised controlled trials comparing terlipressin and vasopressin with octreotide and somatostatin in acute variceal bleeding, with GRADE assessment of certainty | PMID DOI | |
| Somatostatin | Placebo-controlled, double-blind, prospective, randomized study on the effect of octreotide LAR in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors: a report from the PROMID Study Group | 2009 | Phase 3 randomised placebo-controlled trial of the analogue octreotide LAR, not native somatostatin, in 85 patients with metastatic midgut neuroendocrine tumours | PMID DOI Trial | |
| Substance P | Isolation of a sialogogic peptide from bovine hypothalamic tissue and its characterization as substance P | 1970 | Peptide isolation and structural characterisation | PMID | |
| Substance P | Distinct mechanism for antidepressant activity by blockade of central substance P receptors | 1998 | Preclinical work plus a randomised placebo- and paroxetine-controlled clinical trial | PMID | |
| Substance P | The oral neurokinin-1 antagonist aprepitant for the prevention of chemotherapy-induced nausea and vomiting: a multinational, randomized, double-blind, placebo-controlled trial in patients receiving high-dose cisplatin | 2003 | Multinational phase 3 randomised double-blind placebo-controlled trial | PMID | |
| Substance P | Lack of efficacy of the substance P (neurokinin1 receptor) antagonist aprepitant in the treatment of major depressive disorder | 2006 | Report of five randomised double-blind placebo-controlled trials | PMID | |
| Survodutide | BI 456906: Discovery and preclinical pharmacology of a novel GCGR/GLP-1R dual agonist with robust anti-obesity efficacy | 2022 | Preclinical pharmacology: in vitro receptor characterisation and rodent obesity models | Preclinical only | PMID DOI |
| Survodutide | Glucagon and GLP-1 receptor dual agonist survodutide for obesity: a randomised, double-blind, placebo-controlled, dose-finding phase 2 trial | 2024 | 46-week randomised, double-blind, placebo-controlled phase 2 dose-finding trial across 43 centres in 12 countries; 387 adults randomised with BMI at least 27 and without diabetes, 386 treated | PMID DOI Trial | |
| Survodutide | A Phase 2 Randomized Trial of Survodutide in MASH and Fibrosis | 2024 | 48-week randomised, double-blind, placebo-controlled phase 2 trial, 293 adults with biopsy-confirmed steatohepatitis and stage F1-F3 fibrosis, survodutide 2.4, 4.8 or 6.0 mg weekly versus placebo | PMID DOI Trial | |
| Survodutide | Survodutide Once Weekly for the Treatment of Adults with Obesity | 2026 | 76-week randomised, double-blind, placebo-controlled phase 3 trial, 725 adults with obesity (survodutide 3.6 mg n=241, 6.0 mg n=242, placebo n=242); mean baseline BMI 37.9, mean weight 108.8 kg | PMID Trial | |
| Survodutide | Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial | 2026 | 48-week randomised, double-blind, placebo-controlled phase 3 trial with imaging endpoints in adults with obesity and steatotic liver disease | PMID | |
| Tabimorelin | Oral administration of the growth hormone secretagogue NN703 in adult patients with growth hormone deficiency | 2003 | Multicentre, randomised, double-blind, placebo-controlled trial in 97 adults with growth hormone deficiency (83 receiving NN703, 14 placebo); first and last doses of 3 mg/kg with 1.5 mg/kg daily on the six intervening days, giving one week of treatment, followed by a GHRH test three weeks later | PMID DOI | |
| Tabimorelin | The pharmacokinetics, pharmacodynamics, safety and tolerability of a single dose of NN703, a novel orally active growth hormone secretagogue in healthy male volunteers | 2000 | Double-blind, randomised, placebo-controlled single ascending dose study in healthy male volunteers across eight dose levels from 0.05 to 12 mg/kg body weight | PMID DOI | |
| Tabimorelin | A clinical study investigating the pharmacokinetic interaction between NN703 (tabimorelin), a growth hormone secretagogue, and midazolam, a cytochrome P450 3A4 substrate | 2003 | Open interaction study in 17 adult male subjects, each given oral midazolam 7.5 mg on four occasions: at baseline, after a single dose of NN703, after seven days of once-daily NN703, and after a washout period | PMID DOI | |
| Teduglutide | Randomised placebo-controlled trial of teduglutide in reducing parenteral nutrition and/or intravenous fluid requirements in patients with short bowel syndrome | 2011 | Phase 3 multicentre randomised, double-blind, placebo-controlled trial, 83 patients (35 on 0.05 mg/kg/day, 32 on 0.10 mg/kg/day, 16 placebo), 24 weeks | PMID | |
| Teduglutide | Teduglutide reduces need for parenteral support among patients with short bowel syndrome with intestinal failure | 2012 | Phase 3 (STEPS) randomised, double-blind, placebo-controlled trial, 86 patients (43 per arm), 24 weeks | PMID DOI Trial | |
| Teduglutide | Safety and efficacy of teduglutide after 52 weeks of treatment in patients with short bowel intestinal failure | 2013 | 52-week open-label extension of the phase 3 programme | PMID | |
| Teduglutide | Long-term teduglutide for the treatment of patients with intestinal failure associated with short bowel syndrome | 2016 | STEPS-2: 2-year open-label extension of the pivotal STEPS trial, 88 patients enrolled, 65 completed, treatment up to 30 months | PMID | |
| Teduglutide | Teduglutide for the treatment of adults with intestinal failure associated with short bowel syndrome: pooled safety data from four clinical trials | 2020 | Pooled safety analysis across four clinical trials | PMID DOI | |
| Teriparatide | Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis | 2001 | Randomised, double-blind, placebo-controlled phase 3 trial; n=1,637 postmenopausal women with prevalent vertebral fracture; median 21 months. Published as 344(19):1434-41. | PMID DOI | |
| Teriparatide | Effects of teriparatide and risedronate on new fractures in post-menopausal women with severe osteoporosis (VERO): a multicentre, double-blind, double-dummy, randomised controlled trial | 2018 | Multicentre, double-blind, double-dummy, active-controlled randomised trial; n=1,360 postmenopausal women with severe osteoporosis; 24 months. Published as 391(10117):230-240. | PMID DOI | |
| Teriparatide | Teriparatide or alendronate in glucocorticoid-induced osteoporosis | 2007 | Randomised, double-blind, active-controlled trial; n=428 adults on long-term glucocorticoids; 18 months. Published as 357(20):2028-39. | PMID DOI | |
| Teriparatide | Teriparatide and osteosarcoma risk: history, science, elimination of boxed warning, and other label updates | 2022 | Narrative and regulatory review of long-term pharmacovigilance, including linkage of pharmacy claims to state cancer registries. Published as 6(9):e10665. | PMID DOI | |
| Teriparatide | Effect of abaloparatide vs placebo on new vertebral fractures in postmenopausal women with osteoporosis: a randomized clinical trial | 2016 | Randomised, double-blind, placebo-controlled trial with an open-label teriparatide comparator arm; n=2,463 postmenopausal women; 18 months. Published as 316(7):722-33. | PMID DOI Trial | |
| Tesamorelin | Metabolic effects of a growth hormone-releasing factor in patients with HIV | 2007 | Multicentre, randomised, double-blind, placebo-controlled phase 3 trial, n=412, 26 weeks | High-quality evidence | PMID DOI |
| Tesamorelin | Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog, in human immunodeficiency virus-infected patients with excess abdominal fat: a pooled analysis of two multicenter, double-blind placebo-controlled phase 3 trials with safety extension data | 2010 | Pooled analysis of two phase 3 RCTs, n=816, with safety extension to 52 weeks | High-quality evidence | PMID DOI |
| Tesamorelin | Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial | 2019 | Randomised, double-blind, placebo-controlled multicentre trial, n=61, 12 months blinded plus open-label extension | Mixed evidence | PMID DOI Trial |
| Tesamorelin | Effects of growth hormone-releasing hormone on cognitive function in adults with mild cognitive impairment and healthy older adults: results of a controlled trial | 2012 | Randomised, double-blind, placebo-controlled trial; 152 adults enrolled (66 with mild cognitive impairment), 137 completed (76 healthy, 61 with MCI); tesamorelin 1 mg/day subcutaneously for 20 weeks | Mixed evidence | PMID DOI |
| Testagen | Penetration of short fluorescence-labeled peptides into the nucleus in HeLa cells and in vitro specific interaction of the peptides with deoxyribooligonucleotides and DNA | 2011 | In vitro, fluorescence microscopy and oligonucleotide binding, panel of short peptides including KEDG | Preclinical only | PMID DOI |
| Testagen | The Inhibitory Effect and Adsorption Properties of Testagen Peptide on Copper Surfaces in Saline Environments | 2025 | Materials chemistry, electrochemical corrosion inhibition assays on copper | Preclinical only | PMID DOI |
| tetrapeptide-21 | Bioactive tetrapeptide GEKG boosts extracellular matrix formation: in vitro and in vivo molecular and clinical proof | 2011 | In vitro human dermal fibroblast work plus a double-blind randomised placebo-controlled study in 10 volunteers (mean age 48.2) and a separate 30-volunteer three-dimensional fringe projection assessment | PMID DOI | |
| tetrapeptide-21 | Dermal peptide delivery using enhancer molecules and colloidal carrier systems. Part III: Tetrapeptide GEKG | 2018 | In vitro and ex vivo skin permeation study | Preclinical only | PMID |
| tetrapeptide-21 | Elastin-derived peptide hydrogels for sustained dermal delivery of tetrapeptide-21 | 2026 | Formulation and in vitro release/permeation study | Preclinical only | PMID |
| tetrapeptide-21 | Synergistic Effects of Injectable Platelet-Rich Fibrin and Bioactive Peptides on Dermal Fibroblast Viability and Extracellular Matrix Gene Expression: An In Vitro Study | 2025 | In vitro, human dermal fibroblasts | Preclinical only | PMID |
| Thymalin | Peptides of pineal gland and thymus prolong human life | 2003 | Long-term follow-up of 266 elderly participants receiving thymalin, epithalamin or both over 6-8 years; randomisation, blinding and allocation concealment not reported to appraisable standard; volume 24(3-4):233-240 | Limited evidence | PMID |
| Thymalin | [Geroprotective effect of thymalin and epithalamin] | 2002 | Russian-language report on the same cohort of 266 elderly participants followed 6-8 years; volume 10:74-84 | Limited evidence | PMID |
| Thymalin | [Morphological compound and indicators of the blood clotting system in severe COVID-19 patients of middle aged and elderly during treatment of Tocilizumab and Thymalin] | 2022 | Retrospective, non-randomised comparison of three groups (standard care, tocilizumab, thymalin) in severe COVID-19; volume 35(3):368-374 | Limited evidence | PMID |
| Thymalin | Thymalin: Activation of Differentiation of Human Hematopoietic Stem Cells | 2020 | In vitro study of human haematopoietic stem cell differentiation; volume 170(1):118-122 | Preclinical only | PMID DOI |
| Thymalin | The Use of Thymalin for Immunocorrection and Molecular Aspects of Biological Activity | 2021 | Narrative review by the developing group; states thymalin's active short-peptide constituents as EW (thymogen), KE (vilon) and EDP (crystagen); volume 11(4):377-382 | Limited evidence | DOI |
| Thymogen (L-glutamyl-L-tryptophan) | [Application thymogen for preoperative preparation of elderly patients with tumor processes in abdominal cavity] | 2011 | Double-blind, randomised, placebo-controlled trial of preoperative intranasal thymogen for seven days before surgery in elderly patients with abdominal solid tumours; sample size not stated in the accessible abstract; volume 24(2):278-284 | Limited evidence | PMID |
| Thymogen (L-glutamyl-L-tryptophan) | Attenuation of radiation- and chemoradiation-induced mucositis using gamma-D-glutamyl-L-tryptophan (SCV-07) | 2010 | Animal study in golden Syrian hamsters; acute radiation, fractionated radiation, and radiation-plus-cisplatin models; volume 16(7):655-660 | Preclinical only | PMID DOI |
| Thymogen (L-glutamyl-L-tryptophan) | Personalized medicine for mucositis: Bayesian networks identify unique gene clusters which predict the response to gamma-D-glutamyl-L-tryptophan (SCV-07) for the attenuation of chemoradiation-induced oral mucositis | 2011 | Bayesian network analysis of microarray gene expression from blood samples of 28 head and neck cancer patients within an SCV-07 clinical trial population; volume 47(10):951-955 | Limited evidence | PMID DOI |
| Thymogen (L-glutamyl-L-tryptophan) | The effect of thymogen on the state of immunity in destructive pulmonary tuberculosis | 1999 | Russian-language clinical assessment of immune parameters in patients with destructive pulmonary tuberculosis; volume 320(10):65-67, 96 | Limited evidence | PMID |
| Thymogen (L-glutamyl-L-tryptophan) | Thymogen in the treatment of type-1 diabetes mellitus | 1996 | Russian-language clinical assessment of secondary immunodeficiency correction in patients with type 1 diabetes; volume 68(10):12-14 | Limited evidence | PMID |
| Thymosin alpha-1 | The efficacy and safety of thymosin α1 for sepsis (TESTS): multicentre, double blinded, randomised, placebo controlled, phase 3 trial | 2025 | Multicentre, double-blind, randomised, placebo-controlled phase 3 trial, 22 centres in China, enrolling September 2016 to December 2020; n=1106 randomised (552 thymosin α1, 554 placebo); subcutaneous injection every 12 hours for seven days | High-quality evidence | PMID DOI Trial |
| Thymosin alpha-1 | The efficacy of thymosin alpha 1 for severe sepsis (ETASS): a multicenter, single-blind, randomized and controlled trial | 2013 | Multicentre, single-blind, randomised controlled trial, six tertiary teaching hospitals in China; n=361 (181 thymosin α1, 180 control); volume 17(1):R8 | Mixed evidence | PMID DOI Trial |
| Thymosin alpha-1 | Efficacy of thymosin α1 for sepsis: a systematic review and meta-analysis of randomized controlled trials | 2025 | Systematic review and meta-analysis of 11 randomised controlled trials, 1927 patients (967 treatment, 960 control), with subgroup and trial sequential analysis | Mixed evidence | PMID DOI |
| Thymosin alpha-1 | Thymosin alpha1 treatment of chronic hepatitis B: results of a phase III multicentre, randomized, double-blind and placebo-controlled study | 1999 | Phase 3 multicentre, randomised, double-blind, placebo-controlled trial in HBeAg-positive, HBV DNA-positive chronic hepatitis B; n=97 (49 thymosin α1 1.6 mg twice weekly for six months, 48 placebo), with six months' further follow-up; volume 6(5):397-403 | High-quality evidence | PMID DOI |
| Thymosin alpha-1 | The efficacy of thymosin alpha-1 therapy in moderate to critical COVID-19 patients: a systematic review, meta-analysis, and meta-regression | 2023 | Systematic review, meta-analysis and meta-regression of 8 studies searched to March 2023, predominantly retrospective/observational rather than randomised; volume 31(6):3317-3325 | Limited evidence | PMID DOI |
| Thymosin alpha-1 | Comparison of the efficacy of thymosin alpha-1 and interferon alpha in the treatment of chronic hepatitis B: a meta-analysis | 2008 | Meta-analysis of four randomised controlled trials, 199 patients with chronic hepatitis B; thymosin α1 1.6 mg twice weekly versus interferon alfa 5 MU three times weekly over six months; volume 77(2):136-141 | Limited evidence | PMID DOI |
| Thymosin beta-4 | The effect of thymosin treatment of venous ulcers | 2010 | Phase 2 randomised double-blind placebo-controlled dose-escalation, 73 patients randomised across eight European sites (five Italy, three Poland) | Mixed evidence | PMID DOI Trial |
| Thymosin beta-4 | Thymosin beta4 significantly improves signs and symptoms of severe dry eye in a phase 2 randomized trial | 2015 | Multicentre randomised double-masked placebo-controlled Phase 2 at two US sites, 56 days with 28-day follow-up, n=9 (12 treated eyes vs 6 control eyes) | Limited evidence | PMID DOI Trial |
| Thymosin beta-4 | Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-3 | 2019 | Phase 3 randomised placebo-controlled, registered enrolment 700, start 24 May 2019, status completed | Mixed evidence | Trial |
| Thymosin beta-4 | Biological activities of thymosin beta4 defined by active sites in short peptide sequences | 2010 | In vitro and in vivo mapping of thymosin beta-4 fragments including the actin-binding heptapeptide | Preclinical only | PMID DOI |
| Thymosin beta-4 | The beta-thymosin/WH2 domain; structural basis for the switch from inhibition to promotion of actin assembly | 2004 | Structural and biochemical characterisation of the beta-thymosin/WH2 actin-binding module | Preclinical only | PMID DOI |
| Thymosin beta-4 | Thymosin beta-4 is essential for coronary vessel development and promotes neovascularization via adult epicardium | 2007 | Mouse developmental and adult cardiac injury models | Preclinical only | PMID DOI |
| Tirzepatide | Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes | 2021 | Randomised, open-label, active-controlled phase 3 trial, n=1,879, 40 weeks | High-quality evidence | PMID DOI Trial |
| Tirzepatide | Tirzepatide Once Weekly for the Treatment of Obesity | 2022 | Randomised, double-blind, placebo-controlled phase 3 trial, n=2,539, 72 weeks | High-quality evidence | PMID DOI Trial |
| Tirzepatide | Tirzepatide for the Treatment of Obstructive Sleep Apnea and Obesity | 2024 | Two randomised, double-blind, placebo-controlled phase 3 trials, n=469 combined, 52 weeks | High-quality evidence | PMID DOI |
| Tirzepatide | Tirzepatide for Heart Failure with Preserved Ejection Fraction and Obesity | 2025 | Randomised, double-blind, placebo-controlled trial, n=731, median follow-up 104 weeks | High-quality evidence | PMID DOI |
| Tirzepatide | SURMOUNT-5: tirzepatide versus semaglutide in adults with obesity (head-to-head randomised trial) | 2025 | Randomised, open-label, active-controlled phase 3b trial comparing maximum tolerated tirzepatide against semaglutide 2.4 mg weekly over 72 weeks | High-quality evidence | none |
| Tirzepatide | SURPASS-CVOT: cardiovascular outcomes with tirzepatide versus dulaglutide in type 2 diabetes | 2025 | Randomised, double-blind, ACTIVE-COMPARATOR (dulaglutide) cardiovascular outcome trial in type 2 diabetes with atherosclerotic cardiovascular disease | Mixed evidence | none |
| Triptorelin | Comparative efficacy of triptorelin pamoate and leuprolide acetate in men with advanced prostate cancer | 2003 | Randomised, multicentre, active-comparator trial, n=284 (140 triptorelin 3.75 mg, 144 leuprolide 7.5 mg intramuscularly every 28 days for nine injections) | High-quality evidence | PMID DOI |
| Triptorelin | Efficacy and safety of triptorelin 6-month formulation in patients with central precocious puberty | 2016 | International, non-comparative, single-arm phase 3 trial across 18 centres in the US, Chile and Mexico; n=44 treatment-naive children (39 girls, 5 boys), 48 weeks | Mixed evidence | PMID DOI |
| Triptorelin | Efficacy of Testosterone Suppression with Sustained-Release Triptorelin in Advanced Prostate Cancer | 2017 | Pooled retrospective analysis of 920 patients across nine studies of 1-, 3- and 6-month sustained-release triptorelin formulations | Mixed evidence | PMID DOI |
| Triptorelin | Pharmacokinetics of triptorelin after intravenous bolus administration in healthy males and in males with renal or hepatic insufficiency | 1997 | Pharmacokinetic study of a single 0.5 mg intravenous bolus across four groups: healthy men and men with varying degrees of renal or hepatic impairment | Mixed evidence | PMID DOI |
| Vasoactive intestinal peptide (VIP) | Intravenous aviptadil and remdesivir for treatment of COVID-19-associated hypoxaemic respiratory failure in the USA (TESICO): a randomised, placebo-controlled trial | 2023 | Randomised, placebo-controlled factorial platform trial, 28 US sites, 473 participants enrolled April 2021 to May 2022; adults with COVID-19-associated acute hypoxaemic respiratory failure; six-category ordinal outcome at day 90; volume 11(9):791-803 | High-quality evidence | PMID DOI |
| Vasoactive intestinal peptide (VIP) | The Use of IV Vasoactive Intestinal Peptide (Aviptadil) in Patients With Critical COVID-19 Respiratory Failure: Results of a 60-Day Randomized Controlled Trial | 2022 | Randomised controlled trial, 196 patients across ten US hospitals, randomised 2:1 to three days of IV aviptadil or placebo; volume 50(11):1545-1554 | Mixed evidence | PMID DOI Trial |
| Vasoactive intestinal peptide (VIP) | Vasoactive intestinal peptide in man: pharmacokinetics, metabolic and circulatory effects | 1978 | Human study of graded intravenous VIP infusion in healthy volunteers, with plasma VIP measurement and assessment of metabolic and circulatory effects; volume 19(11):1049-1053 | Limited evidence | PMID DOI |
| Vasoactive intestinal peptide (VIP) | VIP Regulates the Development & Proliferation of Treg in vivo in spleen | 2011 | In vivo mouse study using VIP gene-knockout animals, examining regulatory T cell development and proliferation in thymus and spleen; volume 7, article 19 | Preclinical only | PMID DOI |
| Vesugen | Epigenetic aspects of peptidergic regulation of vascular endothelial cell proliferation during aging | 2014 | In vitro, vascular endothelial cell culture during replicative ageing | Preclinical only | PMID |
| Vesugen | Peptide KED: Molecular-Genetic Aspects of Neurogenesis Regulation in Alzheimer's Disease | 2021 | In vitro gene expression analysis | Preclinical only | PMID DOI |
| Vesugen | Peptides tissue-specifically stimulate cell differentiation during their aging | 2012 | Organotypic and cell culture across tissue types, including Vesugen | Preclinical only | PMID DOI |
| Vesugen | Effect of synthetic peptides on aging of patients with chronic polymorbidity and organic brain syndrome of the central nervous system in remission | 2015 | Uncontrolled human observation with multiple peptides administered in combination, Russian language | Limited evidence | PMID |
| Vilon | A synthetic dipeptide vilon (L-Lys-L-Glu) inhibits growth of spontaneous tumors and increases life span of mice | 2000 | Mouse lifespan and spontaneous tumour study | Preclinical only | PMID |
| Vilon | Effect of vilon on biological age and lifespan in mice | 2000 | Mouse ageing biomarker and lifespan study | Preclinical only | PMID DOI |
| Vilon | Peptides Regulating Proliferative Activity and Inflammatory Pathways in the Monocyte/Macrophage THP-1 Cell Line | 2022 | In vitro, human THP-1 monocyte/macrophage line, panel including Vilon (KE) and Epitalon (AEDG) | Preclinical only | PMID DOI |
| Vilon | KE peptide regulates SIRT1, PARP1, PARP2 gene expression and protein synthesis in human mesenchymal stem cells aging | 2023 | In vitro, ageing human mesenchymal stem cell culture | Preclinical only | PMID |
| Vilon | Effects of short peptides on lymphocyte chromatin in senile subjects | 2004 | Ex vivo, lymphocytes from elderly human donors | Preclinical only | PMID DOI |
| Vilon | Peptides of pineal gland and thymus prolong human life | 2003 | Non-randomised open follow-up, 266 elderly subjects, 6-8 years | Limited evidence | PMID |
| voclosporin | A randomized, controlled double-blind study comparing the efficacy and safety of dose-ranging voclosporin with placebo in achieving remission in patients with active lupus nephritis | 2019 | Randomised double-blind placebo-controlled phase 2 dose-ranging trial (AURA-LV), 265 patients at 79 centres in 20 countries, two voclosporin doses versus placebo added to mycophenolate mofetil and rapidly tapered low-dose corticosteroids | PMID DOI | |
| voclosporin | Efficacy and safety of voclosporin versus placebo for lupus nephritis (AURORA 1): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial | 2021 | Randomised double-blind placebo-controlled phase 3, 357 patients (179 voclosporin, 178 placebo) at 142 sites in 27 countries, on background mycophenolate mofetil and low-dose corticosteroids | PMID DOI | |
| voclosporin | Safety and efficacy of long-term voclosporin treatment for lupus nephritis in the phase 3 AURORA 2 clinical trial | 2024 | Blinded continuation of AURORA 1 for a further two years, 216 patients, three years of total treatment | PMID DOI | |
| voclosporin | Update on the efficacy and safety profile of voclosporin: an integrated analysis of clinical trials in lupus nephritis | 2023 | Integrated pooled analysis of the AURA-LV and AURORA 1 randomised trials | PMID DOI | |
| Vosoritide | Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial | 2020 | Randomised, double-blind, placebo-controlled phase 3 trial; n=121 children aged 5 to under 18 with achondroplasia; 24 sites in 7 countries; 52 weeks. Published as 396(10252):684-692. | PMID DOI Trial | |
| Vosoritide | Vosoritide therapy in children with achondroplasia aged 3-59 months: a multinational, randomised, double-blind, placebo-controlled, phase 2 trial | 2024 | Multinational randomised, double-blind, placebo-controlled phase 2 trial; children aged 3 to 59 months with achondroplasia. Published as 8(1):40-50. | PMID DOI Trial | |
| Vosoritide | C-type natriuretic peptide analogue therapy in children with achondroplasia | 2019 | Phase 2 open-label dose-finding and dose-escalation study in children with achondroplasia. Published as 381(1):25-35. | PMID DOI | |
| Vosoritide | Vosoritide treatment for children with hypochondroplasia: a phase 2 trial | 2024 | Single-arm phase 2 trial of vosoritide in children with hypochondroplasia, a milder FGFR3-related skeletal dysplasia. Published as 71:102591. | PMID DOI | |
| Vosoritide | Safe and persistent growth-promoting effects of vosoritide in children with achondroplasia: 2-year results from an open-label, phase 3 extension study | 2021 | Open-label extension of the phase 3 programme; 2-year results. Published as 23(12):2443-2447. | PMID DOI | |
| Ziconotide | Intrathecal ziconotide in the treatment of refractory pain in patients with cancer or AIDS: a randomized controlled trial | 2004 | Randomised, double-blind, placebo-controlled trial; 111 participants with refractory pain due to cancer or AIDS (68 ziconotide, 40 placebo, plus a crossover phase) | PMID DOI | |
| Ziconotide | A randomized, double-blind, placebo-controlled study of intrathecal ziconotide in adults with severe chronic pain | 2006 | Randomised, double-blind, placebo-controlled trial; 220 patients with severe chronic pain (112 ziconotide, 108 placebo), slow titration from 0.1 µg/hour over 3 weeks to a mean of 0.29 µg/hour | PMID DOI |
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