Retatrutide

Phase 3 Clinical Trials

Also known as: LY3437943, Triple G

GLP-1 / Weight LossSubcutaneous

A triple-hormone receptor agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. Shows the highest weight loss of any obesity drug in trials.

Molecular Weight~4700 Da
Half-Life (t½)~6 days
SequenceTriple agonist: GLP-1/GIP/Glucagon receptor

Mechanism of Action

Triple agonism provides complementary metabolic effects: GLP-1 suppresses appetite, GIP enhances insulin sensitivity, glucagon increases energy expenditure and fat oxidation.

Dosing Protocol

Titration from 1mg weekly, increasing monthly to 4mg, 8mg, up to 12mg weekly.

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Reconstitution

Research-grade: 5mg vial + 2mL BAC water.

Storage

Refrigerate 2-8°C. Do not freeze.

Side Effects

  • Nausea
  • Diarrhea
  • Vomiting
  • Constipation
  • Injection site reactions

Key Research Findings

  • Phase 2: up to 24.2% body weight loss at 48 weeks (highest recorded)
  • Superior glycemic control vs semaglutide in early data
  • Significant reduction in liver fat content

Latest Verified Lab Report

No lab reports available for Retatrutide yet.

Community-funded testing results will appear here.

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Research Use Only

This information is provided for educational and research purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional before using any research compounds.