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Retatrutide

Weight Loss & Metabolic

Retatrutide

Investigational once-weekly triple agonist (GIP/GLP-1/glucagon) by Eli Lilly; phase 2 data show large weight loss. Not approved.

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What it is

Retatrutide (LY3437943) is an investigational, once-weekly injectable peptide developed by Eli Lilly. It is a first-in-class "triple agonist" that simultaneously activates the GIP, GLP-1, and glucagon receptors. The glucagon-receptor component is the main feature distinguishing it from dual agonists like tirzepatide, and is thought to add an energy-expenditure effect on top of appetite suppression. In a 48-week phase 2 obesity trial (NEJM, 2023), the highest 12 mg dose produced a mean weight reduction of about 24.2%, among the largest reductions reported for any pharmacologic obesity agent in trials to date. A separate phase 2a trial showed marked reductions in liver fat in people with metabolic dysfunction-associated steatotic liver disease (MASLD). Eli Lilly's phase 3 TRIUMPH program is ongoing. As of mid-2026, retatrutide is NOT approved by the FDA, EMA, or any major regulator and remains an experimental compound under clinical investigation. Material sold by research-chemical vendors is unregulated, not pharmaceutical-grade, and is labeled research-use-only. The data below summarizes published evidence and clearly separates clinical findings from anecdotal community use.

Highlights

  • Substantial body-weight reduction (up to ~24% mean at 12 mg over 48 weeks in the phase 2 obesity trial)
  • Improved glycemic control and metabolic parameters in adults with obesity/overweight
  • Large dose-dependent reductions in liver fat (MASLD), with many high-dose participants reaching normal liver-fat levels at 24 weeks in a phase 2a trial
Read the full research, dosing & citations →

For research use only. Not medical advice.