Petrelintide record · updated 19h ago
Petrelintide is a synthetic peptide that acts as an analogue of human amylin, a hormone co-secreted with insulin by pancreatic beta cells. Its mechanism of action involves binding to the amylin receptors in the brain and peripheral tissues, which leads to a reduction in appetite, slowing of gastric emptying, and modulation of glucose metabolism. These actions collectively contribute to weight loss and improved metabolic outcomes in individuals with obesity.
Development stage
where Petrelintide sits between preclinical work and regulatory approval- 1ClearedPreclinicalAnimal / in-vitro work
- 2ClearedPhase 1Safety in humans
- 3CurrentPhase 2Efficacy signal
- 4Not reachedPhase 3Confirmatory trials
- 5Not reachedApprovedCleared by a regulator
Stage is inferred from the highest trial phase in the indexed corpus. It describes the research record, not a recommendation.
Mass and formula from PubChem CID 172915807. No verified residue count for this compound.
| Study | Type | Year | Summary depth |
|---|---|---|---|
| Initial HIV Therapy for Adults and Treatment-Associated Weight Gain: The Opti-DOR Randomized Clinical Trial. TakeawayNot reported in abstract. | Human | 2026 | Title only0.10 |
| Petrelintide and the evolving role of amylin agonism in obesity. TakeawayNot reported in abstract. | review | 2026 | Title only0.10 |
| Petrelintide, a human amylin analogue for the treatment of obesity (ZUPREME 1): a randomised, double-blind, placebo-controlled, phase 2 trial. Finding-9.8% bodyweight change at 28 weeks with petrelintide 5.0 mg vs -1.7% with placebo. | Human | 2026 | Full text read0.80 |
What people are saying
anecdotal · not evidenceUnverified first-hand accounts from public forums. These are not studies: nobody checked what was taken, whether it was what the label said, or what else was going on. They count for nothing in the evidence grade above and are shown because a reader searching Petrelintide will meet them anyway, and meeting them next to a graded evidence base is better than meeting them alone.