Retatrutide
GIP · GLP-1 · glucagon receptor triple agonist
One engineered peptide that activates three hormone receptors at once. GLP-1 and GIP signaling drive satiety and insulin response, while glucagon-receptor activity is thought to raise energy expenditure and liver fat oxidation. In a 48-week Phase 2 trial, the highest dose produced a mean weight reduction of about 24%.
- Targets
- GIPR · GLP-1R · GCGR
- Structure
- 39-aa peptide, C20 fatty-diacid
- Half-life
- ≈ 6 days
- Status
- Investigational · Phase 3