P Palthera
Hormone Analogues

Retatrutide

LY3437943

Retatrutide (LY3437943) is a single peptide engineered to act at three incretin and metabolic — GIP, GLP-1, and glucagon. It is investigational and not approved as a medicine at the time of writing. Phase II data have been published for obesity and type 2 diabetes; Phase III trials are ongoing.

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Hormone Analogues
Classification
Triple GIP / GLP-1 / glucagon receptor agonist · Investigational (Phase III ongoing)
Research stage
Phase II clinical evidence published; Phase III TRIUMPH and TRIUMPH-OUTCOMES programmes ongoing
Sequence
39-amino-acid lipidated triple-agonist peptide
Molecular weight
Approx. 4731 Da

Snapshot

Key takeaways

A three-bullet snapshot before reading the full dossier.

  1. 01

    Single peptide with combined agonism at GIP, GLP-1, and glucagon .

  2. 02

    Investigational only — not yet FDA-approved at the time of writing.

  3. 03

    Phase II trials reported some of the highest weight-loss magnitudes in incretin-class research to date.

Dossier overview

4

research areas

3

references

3

handling notes

01

Mechanism of action

Retatrutide activates GIP, GLP-1, and glucagon . The combined agonism is associated with the glucose-control and appetite-reduction effects of incretin agents, plus the energy-expenditure effects ascribed to glucagon receptor activation in metabolic research.

02

Research applications

  • Obesity clinical research (Phase II + Phase III)
  • Type 2 diabetes clinical research
  • Multi- incretin pharmacology
  • Glucagon metabolic research

Evidence at a glance

What's behind this profile

3 citations · 2022–2023

Human
3

Studies in human volunteers or patients (incl. early-phase trials).

Publication years

  1. 22
  2. 23
20222023

Counts are derived from the cited studies below. A study covering both in vivo and in vitro work is counted by its primary model. Sample size is reported in 2 of 3 citations. Findings remain model-specific and are not extrapolated to therapeutic use.

03

Study references

Each profile cites a minimum of two peer-reviewed sources, with model type and reported sample size where the source provides it. Findings are model-specific and must not be extrapolated to therapeutic use.

LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept

2022

Coskun T et al. · Cell Metabolism

Model
Preclinical pharmacology and Phase 1 single-ascending-dose study (mouse + human)
Sample
Not reported in abstract

Reported the discovery and Phase 1 first-in-human characterisation of LY3437943, with safety and weight-reduction signals in obese mice and healthy human volunteers.

PMID 35985340 DOI 10.1016/j.cmet.2022.07.013

Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial

2023

Jastreboff AM et al. · New England Journal of Medicine

Model
Phase 2 double-blind RCT in adults with obesity or overweight with comorbidity
Sample
n=338

Retatrutide doses of 4–12 mg were associated with dose-dependent mean body weight reductions of 17.1% to 24.2% versus 2.1% with placebo over 48 weeks.

PMID 37366315 DOI 10.1056/NEJMoa2301972

Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes

2023

Rosenstock J et al. · The Lancet

Model
Phase 2 double-blind RCT in adults with type 2 diabetes
Sample
n=281

Retatrutide doses of 4–12 mg were associated with dose-dependent HbA1c reductions up to 2.02% and body-weight reductions up to 16.94% over 36 weeks.

PMID 37385280 DOI 10.1016/S0140-6736(23)01053-X

Evidence caveats

  • Retatrutide is investigational. Phase III trials (TRIUMPH programme) are ongoing — no Phase III data are published at the time of writing.
  • All published efficacy data are from Phase II trials with limited duration. Long-term safety and cardiovascular outcomes have not been established.

04

Storage and handling

Trial material follows the clinical trial protocol cold-chain. Research-grade material must be stored under controlled laboratory conditions per protocol.

  • Investigational compound — all use is restricted to authorised clinical trials and research settings.
  • Maintain full batch and supplier traceability.
  • Trial product cold-chain follows the relevant clinical trial protocol.

Common questions

Retatrutide FAQ

Plain-English answers backed by the citations on this profile — what it is, what's been studied, regulatory status, evidence limits.

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