Investigational peptide · Triple agonist

Retatrutide: The Complete Research Guide

Retatrutide (LY3437943) is an investigational peptide and triple GIP, GLP-1 and glucagon receptor agonist studied for weight and metabolic outcomes. This guide separates peer-reviewed evidence, new Phase 3 reports and unanswered questions.

Last reviewed: July 2026Evidence gradedFully referenced

Quick facts

The key identifiers and research context in one place.

Compound
Retatrutide
Development code
LY3437943
Developer
Eli Lilly and Company
Class
GIP / GLP-1 / glucagon receptor agonist
Administration in trials
Subcutaneous, once weekly
Regulatory status
Phase 3; not FDA approved
Studied for
Obesity, type 2 diabetes and metabolic conditions

What is retatrutide?

Retatrutide is one molecule engineered to activate three hormone receptors. GLP-1 and GIP signaling overlap with existing incretin medicines; glucagon receptor activity adds a distinct metabolic pathway under study.

In 2023, a Phase 2 obesity trial reported an average 24.2% weight reduction at 48 weeks in the highest-dose group. In 2026, Lilly reported up to 28.3% at 80 weeks in Phase 3 topline results. Neither finding makes retatrutide an approved medicine.

Read the full explainer
24.2%Average reduction at 48 weeks
12 mg · Phase 2
3Receptor targets
GIP · GLP-1 · glucagon
Phase 3Current development stage
Not FDA approved

A focused guide to every major question

Each article distinguishes peer-reviewed findings, trial design and current regulatory facts.

Evidence first. Uncertainty included.

The Retatrutide Guide is an independent educational resource. It is not affiliated with Eli Lilly, is not a vendor and does not recommend unapproved products.

  • Claims linked to primary research
  • Company-reported results clearly labeled
  • Cross-trial limits kept visible
  • Pages reviewed and dated
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