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GLP-1 / Glucagon Co-Agonist

Mazdutide

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Overview

An oxyntomodulin-based dual agonist with Phase 3 programs; not yet broadly approved.

How it works

Mazdutide is a dual agonist that activates both the GLP-1 and glucagon receptors, built on the framework of the natural gut hormone oxyntomodulin.

The GLP-1 arm provides the familiar appetite suppression and insulin effects, while the glucagon arm is thought to raise energy expenditure and improve how the liver handles fat — a two-lever approach to weight and metabolic disease.

It's engineered for once-weekly dosing and is in late-stage development, particularly in China. It remains investigational rather than broadly approved.

Mechanism · Detailed Analysis
Molecular targetA GLP-1 / glucagon dual-receptor agonist based on the gut hormone oxyntomodulin.
Signaling & downstream effectsCombines incretin-driven satiety and insulinotropy with glucagon-receptor signalling thought to raise energy expenditure and improve hepatic lipid handling.
PharmacokineticsAcylated for albumin binding; once-weekly.
CaveatsInvestigational (late-stage development, particularly in China).
Published EvidenceLoading cited studies from PubMed…
Human Data ···

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Animal ···

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In Vitro ···

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Educational aggregation of public literature. Not medical advice and not a recommendation to use any compound. Many compounds here are not approved for human use. Consult a licensed clinician.