Petrelintide
Zealand Pharma
Petrelintide is an experimental amylin analog designed for once-weekly subcutaneous dosing. Amylin is a hormone co-released with insulin that promotes satiety, slows gastric emptying and helps regulate post-meal glucose. Amylin-based drugs interest obesity researchers because they reduce appetite through a mechanism distinct from GLP-1 and other incretin drugs. Zealand Pharma's chemists engineered petrelintide for chemical stability at roughly neutral pH, which they note could allow co-formulation with other peptide drugs in combination therapy. In phase 1 trials it had a half-life of about 10 days and reduced body weight by up to 8.6% after 16 weekly doses. In the ZUPREME 1 phase 2 trial (485 adults with obesity, no type 2 diabetes), once-weekly maintenance doses of 1.0–9.0 mg produced mean weight changes of −7.9% to −9.8% at 28 weeks versus −1.7% on placebo, with reductions of up to −10.7% by week 42. Nausea, mostly mild and during dose escalation, was the most common adverse event (20% vs 6% on placebo); vomiting was infrequent. Petrelintide is investigational, not approved by any regulator, and not legally available for purchase. Its long-term efficacy and safety, and how it performs in combination with incretin drugs, still need phase 3 trials. Approved obesity medicines remain the standard of care; this page is an educational reference.
Specifications
| Origin / Manufacturer | Synthetic amylin analog |
| Active Components | Petrelintide |
| Storage | Not established (investigational) |
| Shelf Life | Not established (investigational) |
| Form Factor | Subcutaneous injection, once weekly (under development) |
Clinical Evidence
Clinical report reference
Clinical report reference
Clinical report reference
Frequently Asked Questions
Sources & References
Every clinical claim on this page traces to a primary peer-reviewed source.
- 1Garvey WT, Ard J, Connery L, et al.. Petrelintide, a human amylin analogue for the treatment of obesity (ZUPREME 1): a randomised, double-blind, placebo-controlled, phase 2 trial. Lancet Diabetes & Endocrinology. 2026;14(11):914-926. doi:10.1016/S2213-8587(26)00213-5 PMID:42810355
- 2Brændholt Olsen M, Griffin J, Hövelmann U, et al.. Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Petrelintide for Weight Management: Two Randomized, Controlled Phase 1 Trials. Diabetes, Obesity and Metabolism. 2026;28(7):5915-5925. doi:10.1111/dom.70753 PMID:42017294
- 3Fischer Munch H, Just R, Mosolff Mathiesen J, et al.. Development of Petrelintide: a Potent, Stable, Long-Acting Human Amylin Analogue. Journal of Medicinal Chemistry. 2025;68(22):23925-23940. doi:10.1021/acs.jmedchem.5c01185 PMID:41217931
Reviewed by
Peptides Academy Editorial
Editorial Team
All clinical claims cross-checked against primary sources. Read our editorial policy →
Related Peptides
Amycretin
Novo Nordisk
An investigational single-molecule GLP-1 and amylin receptor agonist from Novo Nordisk, now named zenagamtide, studied as a once-weekly injection and a once-daily tablet for obesity and type 2 diabetes. It is not approved anywhere.
Cagrilintide
Novo Nordisk
An investigational long-acting amylin analogue from Novo Nordisk, studied alone and with semaglutide (CagriSema). In the phase 3 REDEFINE 1 trial, CagriSema produced a mean 20.4% weight loss at 68 weeks (vs 3.0% on placebo). Not FDA-approved.
CagriSema
Novo Nordisk
CagriSema is Novo Nordisk's investigational once-weekly combination of the amylin analogue cagrilintide 2.4 mg and semaglutide 2.4 mg. It produced 20.4% mean weight loss at 68 weeks in REDEFINE 1; it is not FDA-approved.
Pramlintide
Symlin
Pramlintide (Symlin) is an FDA-approved synthetic analog of amylin, the 37-amino-acid hormone co-secreted with insulin by pancreatic beta cells. Injected subcutaneously before major meals, it is approved only as an add-on to mealtime insulin in type 1 and type 2 diabetes, where it slows gastric emptying, reduces the post-meal rise in glucagon, and reduces food intake. Drugs@FDA now lists the Symlin products as discontinued.
Semaglutide
Ozempic / Wegovy / Rybelsus
Long-acting GLP-1 receptor agonist — FDA-approved for type-2 diabetes and chronic weight management, landmark for its ~15% mean weight reduction in STEP trials.