Mazdutide
IBI362, LY3305677
The first GLP-1 and glucagon dual agonist approved for obesity anywhere in the world, licensed in China while the West is still running trials.
FDA-approved
Approved by China's NMPA in June 2025 for chronic weight management, and again in September 2025 for glycaemic control in type 2 diabetes. Not approved in the United States or Europe, where it remains in trials.
What it is
Mazdutide is an analogue of oxyntomodulin, a naturally occurring gut hormone that activates both the GLP-1 and glucagon receptors. That dual action is the same architecture as survodutide, and one arm short of retatrutide, which adds GIP.
The glucagon arm is what distinguishes this family from semaglutide. GLP-1 agonism suppresses appetite and slows gastric emptying, which reduces energy intake. Glucagon receptor activation raises energy expenditure and mobilises hepatic fat. One side of the equation each.
Why it is the notable one
It got approved first.
China's NMPA licensed mazdutide for chronic weight management in June 2025, making it the first GLP-1 and glucagon dual agonist to receive full regulatory authorisation for obesity anywhere. A second approval for glycaemic control in type 2 diabetes followed in September 2025.
That matters for how this site tiers things. Survodutide and retatrutide are further along in Western trials and better known in English-language communities, and both remain investigational. Mazdutide is approved, with published phase 3 data, and is barely discussed outside China.
Regulatory geography is not a proxy for evidence quality, but it is not nothing either. A drug that has satisfied a major regulator has been through a process that an investigational compound has not.
What the evidence shows
The phase 3 programme in Chinese adults, GLORY for obesity and DREAMS for diabetes, supported both approvals. A US-based phase 2 randomised placebo-controlled trial in adults with obesity or overweight has since been published, which is the step toward a Western filing.
Reported effects beyond weight include reductions in waist circumference, blood lipids, blood pressure, uric acid, liver enzymes and hepatic fat content. The hepatic effects are the ones most plausibly attributable to the glucagon arm rather than to weight loss alone.
Practical notes
- The trial population matters when reading the numbers. The phase 3 data is predominantly Chinese, at BMI thresholds set lower than Western criteria because obesity-related risk appears at lower BMI in East Asian populations. Efficacy figures do not transfer between populations as cleanly as people assume.
- The glucagon arm has a cost. Glucagon receptor activation raises heart rate and can raise hepatic glucose output. This is the same trade being watched in survodutide and retatrutide.
- Do not combine it with another incretin. Same receptor, same class, additive side effects, no additive benefit.
Side effects and warning signs
Commonly reported
- Nausea, most pronounced during titration
- Diarrhoea and vomiting
- Reduced appetite
- Transient rises in heart rate
- Injection-site reactions
Stop and get medical help
- Personal or family history of medullary thyroid carcinoma or MEN2
- Severe persistent abdominal pain radiating to the back
- Signs of gallbladder disease during rapid weight loss
Sources
From the community
Discussion for this compound concentrates in r/Semaglutide.
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