Retatrutide
Limited human dataInvestigational triple-hormone-receptor agonist (GIP + GLP-1 + glucagon receptor agonist peptide) · Also known as LY3437943, GGG tri-agonist, GIP/GLP-1/glucagon triple agonist
Overview
Retatrutide is an investigational once-weekly injectable peptide that activates three receptors at once — GIP, GLP-1, and glucagon — a step beyond the dual GLP-1/GIP mechanism of tirzepatide. In a published Phase 2 obesity trial it produced large average weight reductions (up to roughly 24% at 48 weeks at the highest dose), and a Phase 2a substudy showed substantial reductions in liver fat. The human evidence is genuinely promising but still mid-stage: as of 2026 the pivotal Phase 3 program (TRIUMPH) is ongoing and the drug is NOT FDA-approved for any indication. Developed by Eli Lilly. Treat it as an experimental agent whose long-term efficacy and safety are not yet established.
Commonly Reported Uses
These are uses commonly discussed or marketed by users and vendors — not a list of proven or approved benefits, and not a recommendation.
- Weight loss / obesity (investigational; Phase 2 human data only, not FDA-approved)
- Type 2 diabetes glycemic control (investigational; Phase 2 human data only)
- Metabolic dysfunction-associated steatotic liver disease / liver fat reduction (investigational; Phase 2a human data only)
What to Track
Data points you and your clinician might monitor. For observation only — not a diagnostic protocol.
- Smart scale — weight and body-fat % trend over the measurement period
- InBody/DEXA — skeletal muscle mass vs. fat mass, to watch for lean-mass loss during rapid weight loss
- Labs — HbA1c and fasting glucose if a clinician is monitoring glycemic effects
- Subjective — daily appetite, nausea, and GI tolerability check-ins
- WHOOP — resting heart rate and HRV trend (dose-dependent heart-rate increases were seen in trials)
Sources & References
Quick Reference
- Class
- Investigational triple-hormone-receptor agonist (GIP + GLP-1 + glucagon receptor agonist peptide)
- Evidence Level
- Limited human data
- Reported Uses
- 3 listed
- Tracking Metrics
- 5 suggested
- Citations
- 3 sources
Safety & legal notes
NOT FDA-approved; investigational and only available in clinical trials or, illegitimately, via compounding/gray-market channels that are not quality-controlled. Most common trial side effects were dose-related gastrointestinal events (nausea, vomiting, diarrhea); dose-dependent increases in heart rate were also observed. GLP-1-class incretin agonists are currently on WADA's monitoring program but are NOT prohibited in sport as of the 2026 List; glucagon-receptor activity is a newer mechanism, so athletes should verify current status. Long-term human safety is not established. Consult a licensed clinician.
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