Skip to product information
Retatrutide 30mg — Triple Agonist Peptide for Research Use
Retatrutide is an advanced experimental peptide developed by Eli Lilly, designed as a once-weekly injectable. It is the first compound to simultaneously activate three key metabolic receptors: GLP-1, GIP, and Glucagon — making it a triple agonist with a unique mechanism of action.
How It Works
- GLP-1 Receptor: Reduces hunger signaling, increases satiety, delays gastric emptying, and improves insulin secretion — the same pathway targeted by Semaglutide.
- GIP Receptor: Improves insulin sensitivity, enhances glucose disposal, may reduce GLP-1-associated nausea, and helps preserve lean tissue during weight loss.
- Glucagon Receptor: Mobilizes stored energy, increases fat oxidation, promotes liver-fat reduction, and raises metabolic rate. GLP-1 and GIP activity offsets glucagon's tendency to raise blood glucose.
Clinical Research Highlights
- ~24% weight loss at 48 weeks in Phase 2 obesity studies
- ~28.3% weight loss at 80 weeks with 12mg in Phase 3 TRIUMPH-1
- ~45% of participants achieved ≥30% weight loss
- Significant reductions in visceral and liver fat
- Improved triglycerides, insulin sensitivity, and cardiometabolic markers
Retatrutide vs. Semaglutide vs. Tirzepatide
- Semaglutide: GLP-1 agonist — strong appetite suppression, moderate fat oxidation
- Tirzepatide: GLP-1 + GIP dual agonist — very strong appetite suppression, higher weight loss
- Retatrutide: GLP-1 + GIP + Glucagon triple agonist — highest reported weight loss, greatest fat oxidation studied to date
For research purposes only. Not intended for human use. This product is sold strictly for laboratory and scientific research.