Library / Metabolic Research / Retatrutide
Evidence: Controlled trialsInvestigational (Phase 3)Weight & metabolism

Retatrutide

Investigational triple agonist of the GIP, GLP-1 and glucagon receptors.

39 (modified)Amino acids
~4,731.4Daltons
C₂₂₁H₃₄₂N₄₆O₆₈Formula
2020sResearch period
RetatrutideBackbone of 39 residues. Modified or non-standard residues are not drawn.
CNO

Overview

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In plain language

Retatrutide is an experimental weight-loss medicine from Eli Lilly. It acts on three hormone receptors at once (GIP, GLP-1 and glucagon), which is why it is called a "triple agonist."

In a mid-stage trial, people lost a large amount of weight on average. It is still being tested in large Phase 3 trials and is not FDA-approved. Products sold online as "retatrutide" are not regulated.

Molecular identity

Amino acids
39 (modified)
Molecular weight
~4,731.4 Da
Formula
C₂₂₁H₃₄₂N₄₆O₆₈
Sequence
Modified 39-residue peptide with a fatty diacid chain
Form clarification: Acylated peptide (free form); salt forms differ. Molecular weight is a reference value, not a certificate of analysis.

Origin and history

Retatrutide is Eli Lilly’s next step after tirzepatide: a single molecule that activates three hormone receptors, GIP, GLP-1 and glucagon. Adding glucagon was meant to increase energy burning.

A Phase 2 trial in 2023 reported 24% average weight loss at 48 weeks. In May 2026 the first Phase 3 trial, TRIUMPH-1, reported average weight loss of 28.3% at 80 weeks on the highest dose. It remains investigational and is not approved.

Key people

  • Eli LillyDeveloper
  • Ania JastreboffLead author of the 2023 Phase 2 trial

Timeline

  1. 2022

    First human (Phase 1) results

  2. 2023

    Phase 2: 24% weight loss at 48 weeks

  3. 2026

    Phase 3 TRIUMPH-1: 28.3% weight loss at 80 weeks

See every peptide on one history timeline.

Human evidence

PreclinicalEarly humanControlled trialsApproved use

Phase 3 trials are under way for obesity, type 2 diabetes and related conditions. Results to date are from clinical trials, not approved use.

Registration and enrollment are not proof of benefit; check study results directly.

Explore original publications and distinguish preclinical findings from controlled human evidence.

Safety and regulatory status

See every compound on the regulatory tracker.

Investigational and not FDA-approved. Products sold online as “retatrutide” are unregulated and are not the investigational drug.

This profile is educational and does not provide treatment, dosing or sourcing guidance.

Sources

  1. PubMed literature search: Retatrutide
  2. PubChem compound search: Retatrutide
  3. Jastreboff et al. 2023, NEJM
  4. AJMC: TRIUMPH-1 results (2026)
  5. ClinicalTrials.gov search: Retatrutide
Cite this page

Hernandez Gener, E. (2026, November 7). Retatrutide: molecular data, research history and evidence. VALREXA Biosciences. https://valrexa.com/peptides/retatrutide.html

APA style · Last reviewed November 7, 2026 · Our editorial standards

Last reviewed November 7, 2026. Trial and regulatory status can change; confirm in the linked registries. This profile is educational and is not medical advice, a treatment recommendation, or dosing or sourcing guidance. Report an error · Corrections policy

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