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Tirzepatide

Also sold as Mounjaro, Zepbound.

Half-life
120 h
Steady state
~25 d
Class
GLP-1 / GIP
Category
GLP-1

Published population averages. Steady state is the usual five half-life rule of thumb, not a measurement. See peptide half-life, explained.

Overview

Tirzepatide is a first-in-class dual GLP-1/GIP receptor agonist developed by Eli Lilly. It simultaneously activates both incretin pathways, producing superior glycemic and weight-loss outcomes compared to selective GLP-1 agonists in head-to-head trials. Marketed as Mounjaro (T2DM) and Zepbound (obesity).

How it works

Activates both GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptors. The dual agonism enhances insulin secretion beyond GLP-1 alone, improves lipid metabolism via GIP-mediated adipocyte signaling, and produces stronger appetite suppression through combined hypothalamic and brainstem pathways.

Half-life and peak

Terminal half-life is approximately 5 days (~120 hours), supporting once-weekly dosing. Steady state reached in 4 weeks. Tmax occurs at approximately 8–72 hours post-dose depending on injection site.

What it is studied for

SURPASS clinical program (T2DM), SURMOUNT clinical program (obesity), head-to-head vs semaglutide, cardiovascular and metabolic syndrome outcomes.

Research status

FDA-approved for T2DM (Mounjaro, 2022) and chronic weight management (Zepbound, 2023). SURMOUNT-1 showed up to 22.5% weight loss. Cardiovascular outcomes trial (SURPASS-CVOT) ongoing.

Sources

Educational reference only. This page describes what is published about a compound; it is not medical advice, not a recommendation to take anything, and not a dosing guide. Several compounds in this catalog are investigational and are not approved medicines. Talk to a doctor.

Guides that cover it