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Evidence: AWeight LossMetabolic Health

Retatrutide: Benefits, Dosage & FDA Status

Retatrutide (LY3437943)

Triple agonist at GLP-1, GIP, and glucagon receptors. Phase 2 produced 24.2% mean weight reduction at 48 weeks — the highest ever in a clinical obesity trial.

FDA Status

Not FDA-approved — Phase 3 trials (TRIUMPH program) for obesity

Typical Dose

Trial range: 1–12 mg weekly (subcutaneous)

Evidence Grade

AStrong RCT or FDA-approved evidence

Half-Life

~6 days (estimated)

Routes of Administration

subcutaneous

First Synthesized

2022

Clinics Indexed

12 providers have offered Retatrutide in our tracked directory.

Mechanism of Action

Triple agonist at GLP-1, GIP, and glucagon receptors — combines incretin appetite/glucose actions with glucagon-mediated energy expenditure.

Key Reported Benefits

Benefits listed reflect commonly reported effects from clinical trials and practitioner use. Individual response varies. Evidence-grade A indicates strong rct or fda-approved evidence.

Reported Side Effects

  • Nausea
  • Vomiting
  • Diarrhea
  • Heart-rate increase

Contraindications

  • Personal/family history of medullary thyroid carcinoma
  • Pregnancy

Regulatory & Safety Context

FDA status: Not FDA-approved — Phase 3 trials (TRIUMPH program) for obesity

This page is for educational purposes only and does not constitute medical advice. Peptide use outside of an FDA-approved indication should be discussed with a licensed medical professional. Source quality, cold-chain storage, and injection hygiene all materially affect safety outcomes.

See state-by-state legality: US peptide legality by state →

References

Selected primary literature on Retatrutide. Full PubMed records linked. Additional citations are available on request.

  1. PubMed PMID 37467022

Last reviewed: 2026-04-30

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