Mazdutide

IBI362 · LY3305677 · Innovent/Lilly dual agonist

Rank#999
Weight LossInvestigationalPhase IIIResearchSubQ

Popular for:Weight loss, dual GLP-1/glucagon agonist, Chinese-developed obesity drug

37

Total Studies

23

Human Studies

Phase III

Evidence Level

Investigational

FDA Status

Overview

Mazdutide is a dual GLP-1/glucagon receptor agonist co-developed by Innovent Biologics and Eli Lilly, currently in Phase III clinical trials. It is one of several next-generation obesity drugs competing in the dual/triple agonist space alongside survodutide and retatrutide.

Notably, mazdutide uses bi-weekly (every 2 weeks) dosing rather than weekly, which could be a convenience advantage. Phase II results in Chinese populations showed up to 14.4% weight loss at 24 weeks. It is furthest along in Chinese regulatory pathway and may be among the first dual GLP-1/glucagon agonists to receive approval in any market.

Mechanism of Action

Mazdutide activates both GLP-1 and glucagon receptors, similar to survodutide. The GLP-1 component suppresses appetite and improves glucose metabolism, while glucagon receptor activation increases energy expenditure and hepatic fat oxidation. The bi-weekly dosing is achieved through a modified Fc-fusion structure that extends the half-life beyond typical weekly GLP-1 agonists.

Key Research Benefits

Bi-weekly dosing — most convenient dosing schedule in the class
Up to 14.4% weight loss in Phase II (24 weeks)
Dual GLP-1/glucagon mechanism targets liver fat
Advanced in Chinese regulatory pathway
Backed by Eli Lilly partnership

Clinical Evidence Summary

Research Pipeline

Preclinical
Animal
Phase I
Phase II
Phase III
Approved

37

Total Studies

23

Human Studies

Investigational — Phase III in China, Phase II globally. Co-developed by Innovent Biologics and Eli Lilly. May receive Chinese approval before US/EU submission.

Key Studies / PubMed References

37 studies found on PubMed · showing top 25 by relevance

View all on PubMed

Obesity in China: current progress and future prospects.

Review

Pan XF, Fang ZZ, Zhang L, et al. · The lancet. Diabetes & endocrinology · 2026

PMID: 41389801

IUPHAR review: From foe to friend: Repurposing glucagon to treat obesity and type 2 diabetes.

Review

Elmendorf AJ, Yousefian M, Kim IM, et al. · Pharmacological research · 2026

PMID: 41478576

Novel GLP-1-based Medications for Type 2 Diabetes and Obesity.

Review

Son JW, le Roux CW, Blüher M, et al. · Endocrine reviews · 2026

PMID: 41054801

Mazdutide: First Approval.

Review

Shirley M · Drugs · 2025

PMID: 41028652

Multifunctional incretin peptides in therapies for type 2 diabetes, obesity and associated co-morbidities.

Review

Bailey CJ, Flatt PR, Conlon JM · Peptides · 2025

PMID: 40081498

Side Effects & Safety

GI side effects (nausea, diarrhea, vomiting) — class effect
Decreased appetite
Injection site reactions
Full safety profile not yet established

Known Interactions

No curated interaction entry is live for Mazdutide yet.

Until the interaction table is fully populated, use the interaction checker and related peptides below to explore adjacent compounds and likely research pairings.

Frequently Asked Questions

Research Disclaimer

This page is for research and educational purposes only. The information presented is based on published scientific literature and does not constitute medical advice, diagnosis, or treatment recommendations. Mazdutide is not approved by the FDA for human therapeutic use. Always consult a qualified healthcare professional before making any health-related decisions. The studies referenced are linked to their original PubMed sources for verification.