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In clinical trialsMetabolic ResearchZP8396

Petrelintide

Also known as: ZP8396

An investigational long-acting analog of the pancreatic hormone amylin, developed by Zealand Pharma with Roche. Human data so far come from phase 1 and phase 2 trials reported at conferences and in company releases; rat data come from conference posters.

Evidence: limited · Phase 1-2 human trials, conference-reported; rat posters

At a glance

Class
Long-acting amylin analog
Developer
Zealand Pharma, in collaboration with Roche
FDA status
Investigational. Not approved by the FDA as of October 2026.
Human data
Phase 1 single- and multiple-administration trials; phase 2 ZUPREME-1 (493 adults, 42 weeks) presented at ADA 2026; no full peer-reviewed paper located
Animal / lab data
High-fat-diet model, rats (conference posters, 2024)

Where it’s been studied

123
  • 1Metabolic endpointshigh-fat-diet model, rats (2024 poster)
  • 2Food intake and food choiceHigh-fat-diet model, rats (2024 poster)
  • 3Lean massEchoMRI body composition, rats (2024 poster)

Mechanism studied

Petrelintide is an engineered analog of amylin, a hormone released from pancreatic beta cells together with insulin after meals; it is built for once-weekly use and, per the developer, stays stable without forming fibrils at neutral pH [1]. The developer proposes action at amylin receptors with possible effects on leptin signaling, a mechanism described as distinct from GLP-1 receptor agonists [1]. This proposed mechanism has not yet been detailed in a peer-reviewed paper.

What the research shows

StudyModelReported resultSource
ZUPREME-1, phase 2 [2]Human
493 adults, randomized, double-blind, placebo-controlled, five levels vs placebo, 42 weeks plus follow-up (NCT06662539)
Primary endpoint: prespecified metabolic measure at week 28. Presented at ADA 2026; not yet published in a journalCompany-reported
Zealand Pharma press release 2026
Phase 1 single and multiple administration [3]Human
Single-administration part: 64 healthy men; multiple-administration part: 20 healthy men, 6 weeks; randomized vs placebo
Measured tolerability, gastrointestinal adverse events, steady-state pharmacokinetics and body weight change. Conference posterConference abstract
ADA Scientific Sessions 2024 (1668-P)
Body composition study [4]Rat
High-fat-diet model, rats, n=10 per group, 30 days, vs vehicle and liraglutide
Researchers reported body-weight and body-composition measurements vs vehicle and liraglutide; see poster.Conference abstract
ADA Scientific Sessions 2024 (1662-P)
Food choice study [5]Rat
High-fat-diet model, rats with free access to chow and high-fat diet, n=10 per group, 30 days
Researchers measured high-fat-diet and chow intake vs vehicle; chow intake unchanged in all groups.Conference abstract
ADA Scientific Sessions 2024 (1661-P)

Human trials are listed for research context only; outcomes are reported in the linked publications. Animal and lab results do not establish effects in humans.

Supply

PureLab does not supply this compound. This page summarizes published research only.

More in Metabolic Research

Sources

  1. Zealand Pharma (2026) Source
  2. Zealand Pharma (2026) Source
  3. Griffin J et al. (2024) Source
  4. Vestergaard B et al. (2024) Source
  5. Vestergaard B et al. (2024) Source
For research use only. Not for human or veterinary use. Not a drug, food or cosmetic, and not intended to diagnose, treat, cure or prevent any disease. This library summarizes published research for educational purposes. PureLab Performance Inc.