RETA

Retatrutide

Metabolic Phase 3

Triple agonist targeting GIP, GLP-1, and glucagon receptors. In a phase 2 trial of 338 adults with obesity, the 12 mg dose produced a least-squares mean weight change of -24.2% at 48 weeks versus -2.1% on placebo.

Regulatory status (as of Sept 2026)

Investigational only - no FDA approval for any indication. Not a compoundable substance: it is not on the 503A bulks list, and it was not among the April 2026 Category 2 removals or the July 2026 PCAC votes. Compounded or grey-market 'retatrutide' is unapproved.

See the FDA peptide regulatory tracker · Read our July 27, 2026 dispatch on the FDA PCAC peptide vote
Educational summary. Every effect described below is drawn from the cited published research and describes what was observed in research subjects — not a promise of results, a dose recommendation, or an endorsement for human use. Many peptides are not FDA-approved. Consult a licensed healthcare provider before making any health decision. Full disclaimer.

2 studies referenced · Last reviewed Oct 1, 2026 · Reviewed by The Peptide Dispatch Editorial Team · How we research & label content

TL;DR — Retatrutide at a Glance

Retatrutide is an investigational drug in late-stage (phase 3) human trials. Triple agonist targeting GIP, GLP-1, and glucagon receptors.

Half-lifeAbout 6 days
How it's given in studiesSubcutaneous injection
Research stagePhase 3
Dosing
Published research: 1, 4, 8 or 12 mg subcutaneously once weekly for 48 weeks in a phase 2 double-blind placebo-controlled trial…
details1, 4, 8 or 12 mg subcutaneously once weekly for 48 weeks in a phase 2 double-blind placebo-controlled trial of 338 adults with obesity (escalation from 2 mg or 4 mg starting doses)
Community-reportedCommunity-reported: 1–12 mg weekly, subcutaneous injection

Published-research dosing is what was given in the cited studies (species and units as reported). Community-reported dosing is what users describe, not from clinical studies. Neither is a recommendation. Not medical advice.

Where each point comes from: Clinicalhuman trials and FDA labels   Lab / animalrodent, cell and ex vivo studies   Community-reporteduser experience and commonly used protocols, not from clinical studies

How It Works

In plain terms: It acts on three gut-hormone receptors (GIP, GLP-1 and glucagon) and led to weight loss in a clinical trial. Agonist of the GIP, GLP-1 and glucagon receptors (Jastreboff 2023). Its effect on body weight comes from a 48-week phase 2 RCT in 338 adults with obesity, in which mean weight change at 48 weeks ranged from -8.7% (1 mg) to -24.2% (12 mg) vs -2.1% with placebo (Jastreboff 2023).

Effects Reported in Research

How to read this: Each item below is an effect observed in research subjects in the cited studies — think of Dexter, our stand-in research subject. These are findings from the literature, not results you should expect, and not medical advice.

  • ClinicalWeight loss in a phase 2 trial (n=338 adults with obesity): least-squares mean change of -24.2% at 48 weeks on 12 mg vs -2.1% on placebo

What Users Report (Community, Not Clinical)

Commonly reported protocol

Community-reportedIn user communities, Retatrutide is typically run at 1–12 mg weekly (subcutaneous injection). This is not a recommendation.

What users report

  • Community-reportedMetabolic improvements
  • Community-reportedPotential for fatty liver treatment

Community reports are anecdotal, vary widely in product quality and purity, and are not medical advice. Talk to a licensed provider.

Side Effects and Safety Notes

  • Gastrointestinal events (nausea, diarrhoea, vomiting) were the most common, dose-related, mostly mild to moderate, and partly mitigated by a 2 mg rather than 4 mg starting dose
  • Dose-dependent increases in heart rate that peaked at 24 weeks and declined thereafter
  • Long-term safety is not established; phase 3 outcome data are pending

References

  1. Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial
    Jastreboff AM, Kaplan LM, Frías JP, Wu Q, Du Y, Gurbuz S et al. The New England journal of medicine. 2023. PMID: 37366315.
    Study type: Phase 2 double-blind randomized placebo-controlled trial, n=338 adults with obesity, 48 weeks.
    DOI: 10.1056/NEJMoa2301972 · PubMed
  2. The First Triple Agonist for Antiobesity: Retatrutide
    Tetelbaun L, Mullally JA, Frishman WH. Cardiology in review. 2024. PMID: 39724554.
    Study type: Review of phase 1 and 2 clinical trial data.
    DOI: 10.1097/CRD.0000000000000793 · PubMed

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How Retatrutide Compares

PeptideHalf-LifeRouteResearch Status
Retatrutide~6 daysSubcutaneous injectionPhase 3
5-Amino-1MQUnknownOralPreclinical (animal)
AOD-9604No published PK data foundSubcutaneous injectionDiscontinued
Adipotide (FTPP)No published PK data foundSubcutaneous injectionPreclinical (animal)
Dulaglutide~5 daysSubcutaneous injectionFDA-approved

Values reflect figures reported in published research. Compare any peptides side-by-side →

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Frequently Asked Questions

What is Retatrutide?
Triple agonist targeting GIP, GLP-1, and glucagon receptors. In a phase 2 trial of 338 adults with obesity, the 12 mg dose produced a least-squares mean weight change of -24.2% at 48 weeks versus -2.1% on placebo.
How does Retatrutide work?
In plain terms: It acts on three gut-hormone receptors (GIP, GLP-1 and glucagon) and led to weight loss in a clinical trial. Agonist of the GIP, GLP-1 and glucagon receptors (Jastreboff 2023). Its effect on body weight comes from a 48-week phase 2 RCT in 338 adults with obesity, in which mean weight change at 48 weeks ranged from -8.7% (1 mg) to -24.2% (12 mg) vs -2.1% with placebo (Jastreboff 2023).
What is the research status of Retatrutide?
Retatrutide is at the following stage in the published literature: Phase 3. All information is for research and educational purposes only.
What is the half-life of Retatrutide?
Reported half-life: ~6 days.
How is Retatrutide administered in research?
Reported administration route in the literature: Subcutaneous injection. This is not a recommendation for human use.

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Category

This peptide belongs to the Metabolic category. View All Metabolic Peptides

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Sources & Methodology

Dosing, half-life figures, and mechanism descriptions on this page are compiled from peer-reviewed published research, with the species and study type stated where reported. Figures labeled “Dosing used in published research” describe what was given in those studies and do not constitute dosing recommendations for any human use. Each cited paper is listed with DOI and PubMed links in the References section above. Found an error? Contact us.

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