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InvestigationalWeight lossSubcutaneousEvidence 4/5

Retatrutide

Also known as: LY3437943

Activates GLP-1, GIP and glucagon receptors simultaneously to suppress appetite and raise energy expenditure.

This page is a structured profile. Narrative evidence, dosing context and FAQs live on the research guide — not duplicated here as a second full article.

Illustrative subcutaneous database profile for Retatrutide
Illustrative profileSubcutaneous
Database profileInvestigational
RetatrutideWeight loss
Drug class
Triple agonist (GLP-1 / GIP / glucagon)
Primary targets
GLP-1R, GIPR, GCGR
Dose reference
1–12 mg once weekly (trial)
Half-life
~6 days
Developer / origin
Eli Lilly
Reference year
2023
Evidence score
4/5 - Phase 2 human evidence
Evidence 4/5

Phase 2 human evidence

Retatrutide has randomized phase 2 human data in obesity and type 2 diabetes, but it remains investigational and is not an approved drug.

Investigational compound with human randomized or phase 2/3 evidence.

Evidence basis

  • Human phase 2 obesity trial
  • Human type 2 diabetes phase 2 trial
  • No approved indication yet

How to read this entry

Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.

Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.

Retatrutide guides

Read the matching guide or adjacent research pages for more context.

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