Metabolic · FDA Approved
Tirzepatide (Mounjaro/Zepbound)
FDA-approved
01 · Overview
A once-weekly dual glucose-dependent insulinotropic polypeptide (GIP) and GLP-1 receptor agonist. Tirzepatide activates both incretin pathways, and in head-to-head trials produced greater HbA1c lowering and weight loss than the selective GLP-1 RA semaglutide in type 2 diabetes (PMID 34170647).
In adults with obesity without diabetes, it also produced greater weight and waist reduction than semaglutide (PMID 40353578).
02 · Research summary & key findings
SURMOUNT-1 showed mean body weight reductions of 15.0% to 20.9% at 72 weeks across doses versus 3.1% with placebo (PMID 35658024). SURPASS-2 demonstrated superior HbA1c reduction vs. semaglutide (PMID 34170647), and SURMOUNT-5 showed 20.2% vs. 13.7% weight loss vs. semaglutide in obesity (PMID 40353578). FDA-approved for type 2 diabetes (Mounjaro, 2022) and chronic weight management (Zepbound, 2023).
03 · Regulatory status
Tirzepatide (Mounjaro/Zepbound) has received FDA approval and is available for clinical use under appropriate medical supervision. Consult a qualified healthcare provider for prescribing information.
04 · Administration routes
- Subcutaneous injection (weekly)
References
- [1]Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes N Engl J Med, 2021. PMID 34170647
- [2]Tirzepatide Once Weekly for the Treatment of Obesity N Engl J Med, 2022. PMID 35658024
- [3]Tirzepatide as Compared with Semaglutide for the Treatment of Obesity N Engl J Med, 2025. PMID 40353578
Primary literature
- PubMed: "Tirzepatide"
Peer-reviewed literature indexed by the National Library of Medicine.
- ClinicalTrials.gov: "Tirzepatide"
Registered interventional and observational studies, including status and phase.
- PubChem: "Tirzepatide"
Chemical structure, molecular properties, and bioactivity data.
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