Dual GLP-1/GIP agonist — produces the greatest average weight loss of any approved medication.
Tirzepatide is a dual GLP-1/GIP receptor agonist developed by Eli Lilly. The SURMOUNT trials demonstrated average weight loss of 20.9% of body weight — exceeding semaglutide and approaching bariatric surgery outcomes. Approved as Mounjaro (diabetes) and Zepbound (obesity).
Mechanism: Tirzepatide activates both GLP-1 receptors (appetite suppression, slowed gastric emptying, insulin secretion) and GIP receptors (enhanced insulin secretion, fat cell metabolism, potential additive appetite suppression). The dual mechanism produces synergistic weight loss beyond either hormone alone.
| Week | Dose | Notes |
|---|---|---|
| 1–4 | 2.5 mg/week | Starting dose — always begin here |
| 5–8 | 5 mg/week | First escalation |
| 9–12 | 7.5 mg/week | Mid-range therapeutic dose |
| 13–16 | 10 mg/week | Most patients see strong response here |
| 17–20 | 12.5 mg/week | Near-maximum dose |
| 21+ | 15 mg/week | Maximum approved dose |
| Maintenance | 5–15 mg/week | Lowest dose that maintains results |
Tirzepatide titration is every 4 weeks — the slowest GLP-1 titration schedule, reflecting its potency. Many clinicians extend each step to 6–8 weeks for better tolerability. Unlike semaglutide's flat titration, many patients find their 'sweet spot' dose between 7.5–12.5 mg and stay there rather than pushing to 15 mg. Same-day weekly injection, rotate sites.