Mazdutide Research Overview (also known as IBI362, OXM3, GLP-1/glucagon dual agonist, Mazdutide peptide)

At a glance

Mazdutide is a dual agonist of GLP-1 and glucagon receptors, developed by Innovent Biologics under the code IBI362. The page examines its role in obesity and metabolic research. Topics include body weight, diabetes, cardiovascular questions and liver-fat biology, distinguishing its dual-receptor mechanism from GLP-1 receptor activation alone.

What Is Mazdutide?

Mazdutide (IBI362/OXM3) is a once-weekly injectable dual agonist of GLP-1 and glucagon receptors developed by Innovent Biologics. Unlike pure GLP-1 agonists, Mazdutide's glucagon receptor component adds energy expenditure enhancement and hepatic fat reduction, positioning it as both an obesity and NASH (non-alcoholic steatohepatitis) treatment candidate.

Dual Mechanism Advantage

GLP-1 receptor agonism provides appetite suppression, glucose-dependent insulin secretion, and slowed gastric emptying. Glucagon receptor agonism adds increased energy expenditure through thermogenesis and lipolysis, and — most distinctively — direct reduction of hepatic fat through glucagon's ability to drive liver fat oxidation. The combination produces weight loss that includes preferential liver fat reduction, addressing the hepatic component of metabolic syndrome that pure GLP-1 agonists address less directly.

Clinical Data

Phase 2 trials reported mean weight losses of approximately 10–11% body weight over 24 weeks in adults with obesity or overweight. In subjects with T2D, significant HbA1c reductions were observed alongside weight loss. Phase 3 trials in obesity and NASH are ongoing.

Quick Reference

Member reference tables summarize the compound's research parameters.

Sign in to view this section

Research Indications

Weight Loss
Preliminary Data

Severe Obesity Management

GLORY-2 trial: 20.1% weight loss with 9mg dose over 60 weeks. 48.7% achieved ≥20% weight reduction

Metabolic Syndrome Improvement

Significant reductions in waist circumference, blood pressure, triglycerides, LDL cholesterol, and uric acid

Liver Fat Reduction

80.2% reduction in liver fat content in exploratory analysis, suggesting potential MASLD benefits

Diabetes
Preliminary Data

Type 2 Diabetes Management

HbA1c reductions of 1.41-2.03% across trials. Superiority vs semaglutide demonstrated in DREAMS-3

Dual Endpoint Achievement

48% achieved both HbA1c <7.0% AND ≥10% weight loss vs 21% with semaglutide

Cardiovascular
Preliminary Data

Blood Pressure Reduction

Consistent reductions in systolic (-7.57 mmHg) and diastolic (-2.98 mmHg) blood pressure

Lipid Profile Enhancement

Improvements in total cholesterol (-16.82%), triglycerides (-43.29%), and LDL (-17.07%)

Research Protocols

As reported in cited literature and research-community logs (see Research Citations below), not a personal dosing recommendation.

This member section describes parameters reported in the research literature.

Sign in to view this section

Peptide Interactions

This member section summarizes reported compound interactions and evidence limitations.

Sign in to view this section

Reported Research Time Points

This member section summarizes reported research time points.

Sign in to view this section

Safety Notes

Included for harm-reduction awareness only, in the event this compound is encountered outside its labeled research use. Inclusion here does not imply RUO Codes endorses, recommends, or instructs human use.

This member section discusses research safety considerations and uncertainties.

Sign in to view this section

Quality Indicators

Verified Marker

White lyophilized powder

Light, fluffy powder without clumping or discoloration

Verified Marker

Clear reconstituted solution

Completely clear and colorless after proper reconstitution

Quality Concern

Cloudy or particles visible

Indicates degradation - do not use

Research Citations

Research Focus

Weight loss, GLP-1/glucagon dual agonism, Type 2 diabetes, Metabolic health, Liver fat reduction

Verified Vendors Carrying Mazdutide

Related Compounds

Related Articles

Browse all peptides in the Encyclopedia →