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Mazdutide

The world's first approved dual GLP-1/glucagon receptor agonist, developed by Innovent Biologics (China). Approved in China for obesity and type 2 diabetes. Phase 3 trials showed up to 20.1% weight loss.

ModerateLimited Data

What is Mazdutide?

Mazdutide (IBI362/LY3305677, brand name Xinermei) is a synthetic oxyntomodulin analog with a C18 fatty acid side chain enabling once-weekly subcutaneous dosing. It is a dual agonist of both GLP-1 and glucagon receptors — the same mechanism as survodutide but developed independently by Innovent Biologics in China, with Eli Lilly holding rights outside China. In June 2025, it became the world's first approved dual GCG/GLP-1 receptor agonist when China's NMPA approved it for weight management, followed by type 2 diabetes approval in September 2025. Phase 3 trials showed up to 20.1% weight loss at 9 mg (GLORY-2) and in a head-to-head trial against semaglutide, 48% vs 21% of patients achieved the combined endpoint of HbA1c <7% plus 10%+ weight loss. It is not FDA or EMA approved and no US filing has been announced.

Why People Talk About It

Weight loss rivaling tirzepatide (up to 20.1%)

Moderate

Superior glycemic control vs semaglutide in head-to-head trial

Moderate

First-in-class dual GCG/GLP-1 agonist approval

Moderate

Glucagon-mediated energy expenditure increase

Emerging

How It Works

Mazdutide activates two receptors: GLP-1 (which reduces appetite and improves blood sugar) and glucagon (which increases energy expenditure and promotes fat burning in the liver). The combination means you eat less AND burn more — a dual approach that neither receptor alone achieves as effectively.

Common Questions

Safety Information

Important Safety Notes

Common Side Effects

Nausea (most common, dose-dependent)VomitingDiarrheaDecreased appetiteGenerally mild to moderate GI effects consistent with GLP-1 drug class

Cautions

  • Approved only in China — not FDA or EMA approved
  • GI side effects are dose-dependent; slower titration improves tolerability
  • Glucagon receptor activation may raise hepatic glucose output transiently
  • Long-term safety data beyond clinical trial durations is limited

What We Don't Know

Cardiovascular outcomes data is not yet available. Whether the glucagon component confers additional liver or metabolic benefits beyond GLP-1 alone in long-term use is still being studied. Western market safety data and regulatory review have not occurred.

Published Research

9 studies

Related Peptides

Quick Facts

Class
Incretin Mimetic
Evidence
Moderate
Safety
Limited Data
Updated
Apr 2026
Citations
9PubMed

Also known as

IBI362LY3305677Xinermei

Tags

GLP-1/Glucagon AgonistWeight LossDual AgonistType 2 DiabetesInnovent BiologicsChina Approved

Evidence Score

Overall Confidence65%

Clinical Trials

View Clinical Trials

Links to ClinicalTrials.gov for reference. Listing does not imply endorsement.