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Petrelintide
GLP-1 Analogs

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 / ManufacturerSynthetic amylin analog
Active Components
Petrelintide
StorageNot established (investigational)
Shelf LifeNot established (investigational)
Form FactorSubcutaneous injection, once weekly (under development)

Clinical Evidence

Phase 1 (Brændholt Olsen et al., Diabetes Obes Metab 2026): single- and multiple-ascending-dose trials. Petrelintide was slowly absorbed, had a half-life of about 10 days, and reduced body weight by up to 8.6% after 16 weekly doses escalated to 2.4–9.0 mg. Nausea occurred in 16.7–33.3% of participants on petrelintide versus 16.7% on placebo in the longer trial part; there were no serious or severe treatment-emergent adverse events.

Clinical report reference

Phase 2 ZUPREME 1 (Garvey et al., Lancet Diabetes Endocrinol 2026; 485 adults with obesity or overweight with comorbidity, without type 2 diabetes): mean weight change at 28 weeks was −7.9% (1.0 and 2.5 mg), −9.8% (5.0 mg), −9.3% (7.0 mg) and −9.4% (9.0 mg) versus −1.7% on placebo, with reductions up to −10.7% at week 42. Nausea affected 20% on petrelintide versus 6% on placebo; vomiting 3% versus 6%; diarrhoea and constipation were similar to placebo.

Clinical report reference

Both trials were sponsored by Zealand Pharma. Phase 3 data, longer follow-up, body-composition results and combination studies with incretin drugs are not yet published.

Clinical report reference

Frequently Asked Questions

Sources & References

Every clinical claim on this page traces to a primary peer-reviewed source.

  1. 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
  2. 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
  3. 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

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Peptides Academy Editorial

Editorial Team

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