CagriSema
Human dataCagrilintide plus semaglutide — the only compound in this class built on amylin rather than a second incretin receptor. Strong Phase 3 numbers, and it lost the one head-to-head trial it ran.
Every compound this site covers, organized by what it is studied for. The badge on each card states the evidence class honestly: a compound with only rodent data says so. Each guide cites its primary sources, and the research database holds every citation in one filterable list.
Cagrilintide plus semaglutide — the only compound in this class built on amylin rather than a second incretin receptor. Strong Phase 3 numbers, and it lost the one head-to-head trial it ran.
GIP/GLP-1/glucagon triple agonist in Phase 3 trials. The strongest human evidence base of any compound covered here, and not yet approved.
GLP-1 agonist approved as Wegovy and Ozempic. The deepest evidence base in the class, including cardiovascular outcome data.
Glucagon/GLP-1 dual agonist (BI 456906). The weakest weight numbers of the new generation — and the strongest liver-disease data, which is arguably its real indication.
GIP/GLP-1 dual agonist approved as Zepbound and Mounjaro — the strongest results of any currently prescribable weight-loss drug.
Gastric pentadecapeptide with an extensive rodent literature on gut, tendon and nerve healing — and no controlled human trial.
The blend vial sold as a repair stack. No study has tested the two compounds in combination.
Synthetic fragment of thymosin β4. The parent protein reached human trials; the fragment sold as a research chemical has not.
GHRH analog sold in two forms that behave nothing alike: with DAC a single dose lasts days, without DAC about thirty minutes. Human studies measured hormone levels, never outcomes.
GHRH analog plus selective ghrelin agonist. Small human pharmacology studies exist for each compound; no outcome trial of the blend.
Orally active ghrelin mimetic — not a peptide. Unusually well studied for this catalog: a two-year randomized trial, a failed Alzheimer's trial, and a hip-fracture trial stopped early for a heart-failure signal.
GHRH(1-29) — a formerly FDA-approved drug (Geref) for pediatric growth hormone deficiency, discontinued for business reasons. The anti-aging use rests on hormone-level studies, not outcome trials.
The only GHRH analog with a current FDA approval — Egrifta, for excess abdominal fat in HIV-associated lipodystrophy. Full Phase 3 program, liver-fat and muscle data.
Mitochondrially encoded peptide with animal metabolic data; human data is observational only.
Cardiolipin-binding mitochondrial peptide: FDA approved as FORZINITY for Barth syndrome in 2025, and separately failed its Phase 3 trial in primary mitochondrial myopathy.
Copper tripeptide with strong in-vitro collagen data, one largely negative randomised human trial of the topical form, and no human data for the injected form.
A pre-mixed three-peptide blend sold for skin and recovery. No study has tested the combination; the evidence for each component is separate and mostly preclinical.
Non-selective melanocortin agonist, never approved anywhere. The human evidence is early trials plus a series of published adverse-event case reports.
Melanocortin agonist approved as Vyleesi for HSDD in premenopausal women. Full human trial program and an FDA label.
α-MSH C-terminal tripeptide studied in cell and mouse models of intestinal inflammation. Preclinical only.
NNMT inhibitor — not a peptide. Mouse fat-loss and muscle data; no human trial published or registered.
Angiotensin IV-derived compound studied for cognition in rodents. The paper behind its famous potency claim was retracted in 2025, and no human trial has ever been published.
GH fragment studied for lipolysis in mice; the human phase 2 obesity data exists only in company disclosures. Covered in the fat-loss rankings.