For laboratory and research use only. Not for human consumption.
Weight Loss

Mazdutide

Also known as: IBI362, LY3305677

Clinical Trials
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Key Facts: Mazdutide

Category
Weight Loss
FDA Status
Not FDA Approved
Clinical Status
Approved in China (NMPA) for chronic weight management since June 2025 and for glycemic control in type 2 diabetes since September 2025. Not FDA or EMA approved. Developed by Innovent Biologics with Eli Lilly.
Banned in Sport (WADA)
Not named on the WADA list, and its approval in China means the S0 catch-all does not apply, so it is not prohibited (2026).
Administration
Subcutaneous injection, once weekly
Typical Dose
4-6 mg weekly
Frequency
Once weekly
Duration
Ongoing weekly use in trials, typically assessed at 24 to 48 weeks
Also Known As
IBI362, LY3305677

How does Mazdutide work?

Two receptors, two jobs. The GLP-1 arm does the familiar work: it suppresses appetite, slows gastric emptying and improves glucose-dependent insulin release. The glucagon arm is the interesting half, because glucagon is normally thought of as the hormone that raises blood sugar. At these doses the intent is to exploit glucagon's other effects, increasing energy expenditure and pushing the liver to burn fat, while the GLP-1 arm keeps blood glucose in check and cancels out glucagon's hyperglycemic tendency. That balance is the whole design: glucagon supplies extra fat burning that GLP-1 alone cannot, and GLP-1 supplies the safety margin that makes adding glucagon viable. Reported reductions in liver fat are consistent with the glucagon component doing what it is meant to.

What does the research show?

The pivotal trial is GLORY-1, published in the New England Journal of Medicine in 2025: 610 Chinese adults with overweight or obesity over 48 weeks. Mean weight reduction was 11.0 percent at 4 mg and 14.0 percent at 6 mg, alongside improvements in liver fat, blood pressure and lipids. A 9 mg dose has since been studied in phase 2 (about 12.8 percent at 24 weeks) and is in phase 3. Tolerability followed the pattern of the whole class, dominated by dose-dependent nausea, vomiting and diarrhea during titration. One caveat matters when reading these numbers: GLORY-1 enrolled a population with a mean BMI of 31.1, against roughly 38 in the Western trials of semaglutide and tirzepatide, so the percentages are not directly comparable to SURMOUNT-1 or STEP-1 results. There is no completed Western phase 3 program, so neither the FDA nor the EMA has assessed it, and meaningful head-to-head data against tirzepatide or retatrutide does not exist.

Trial Progress:Preclinical
Pre
I
II
III
IV
FDA

What doses have been studied?

Human Trials·Phase 3 complete and approved in China. No FDA or EMA assessment.

Typical Dosingⓘ

Community experience

Common Dose

4-6 mg weekly

Range

1.5-9 mg weekly, escalated upward

Frequency

Once weekly

Trial protocols escalated over several weeks rather than beginning at a maintenance amount, and the nausea and vomiting behind most discontinuations is concentrated in that escalation window.

Research Dosingⓘ

Scientific studies

Doses from the Chinese phase 3 program

Duration

Ongoing weekly use in trials, typically assessed at 24 to 48 weeks

Administration

Subcutaneous injection, once weekly

When and how is Mazdutide taken?

Best Time to Take

Same day each week, morning preferred

Once weekly

Food Recommendation

With or without food

Why This Timing?

Weekly dosing means consistency of day matters more than time. Morning allows side effects to be noticed and managed during waking hours.

What are the side effects of Mazdutide?

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • ●Nausea, worst during dose escalation
  • ●Vomiting
  • ●Diarrhea
  • ●Decreased appetite (the intended effect, but can be excessive)
  • ●Injection site reactions
  • ●Increased heart rate
  • ●Gallbladder-related events, as seen across the class

References

Research This Peptide Further

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Frequently Asked Questions

What does Mazdutide do?

Mazdutide is a GLP-1 and glucagon dual agonist, which puts it between semaglutide (GLP-1 only) and retatrutide (GLP-1, GIP and glucagon). It is built on oxyntomodulin, a natural gut hormone that hits both receptors, rather than on a GLP-1 backbone. It is furthest along in China, where it is approved for both weight management and type 2 diabetes. Western approval has not happened.

How does Mazdutide work?

Two receptors, two jobs. The GLP-1 arm does the familiar work: it suppresses appetite, slows gastric emptying and improves glucose-dependent insulin release. The glucagon arm is the interesting half, because glucagon is normally thought of as the hormone that raises blood sugar. At these doses the intent is to exploit glucagon's other effects, increasing energy expenditure and pushing the liver to burn fat, while the GLP-1 arm keeps blood glucose in check and cancels out glucagon's hyperglycemic tendency. That balance is the whole design: glucagon supplies extra fat burning that GLP-1 alone cannot, and GLP-1 supplies the safety margin that makes adding glucagon viable. Reported reductions in liver fat are consistent with the glucagon component doing what it is meant to.

Is Mazdutide FDA approved?

No, Mazdutide is not currently FDA approved. Current status: Approved in China (NMPA) for chronic weight management since June 2025 and for glycemic control in type 2 diabetes since September 2025. Not FDA or EMA approved. Developed by Innovent Biologics with Eli Lilly.

Is Mazdutide banned in sport?

Not named on the WADA list, and its approval in China means the S0 catch-all does not apply, so it is not prohibited (2026).

What are the side effects of Mazdutide?

Reported side effects include: Nausea, worst during dose escalation, Vomiting, Diarrhea, Decreased appetite (the intended effect, but can be excessive), Injection site reactions. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of Mazdutide?

Community-reported common dose: 4-6 mg weekly (Once weekly). Range: 1.5-9 mg weekly, escalated upward. Administration: Subcutaneous injection, once weekly. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with Mazdutide or used in similar applications.

Semaglutide

FDA

Semaglutide is a GLP-1 receptor agonist, a peptide engineered to mimic the natural gut hormone GLP-1 but with a roughly week-long half-life so it can be dosed once weekly. It is FDA-approved and sold as Ozempic and Rybelsus for type 2 diabetes and as Wegovy for chronic weight management, with cardiovascular benefit also on the label. This is one of the most rigorously tested peptides in existence, backed by large randomized trials, so the evidence here is in a completely different league from research-only peptides.

Weight Loss

Tirzepatide

FDA

Tirzepatide is a single peptide that activates two receptors at once: GIP and GLP-1, the two main incretin hormones your gut releases after eating. It is FDA-approved as Mounjaro for type 2 diabetes and as Zepbound for chronic weight management and obstructive sleep apnea, and it has produced the largest weight-loss numbers of any approved drug to date. Like semaglutide, this is a heavily trialed, fully approved medicine, not a gray-market research compound.

Weight Loss

Retatrutide

Clinical Trials

Retatrutide is the heavy hitter of the new weight-loss drugs: a once-weekly injectable peptide that hits three receptors at once - GIP, GLP-1, and glucagon - earning it the nickname triple-G agonist. In phase 2 it produced about 24 percent weight loss at the top dose, and in the phase 3 TRIUMPH-1 trial Lilly reported 28.3 percent at 12 mg over 80 weeks. It is investigational, made by Eli Lilly, and not FDA approved; Lilly plans to file with the FDA in the first quarter of 2027. Because it is not an approved drug, FDA says it cannot be legally compounded.

Weight Loss

Orforglipron

FDA

Orforglipron is Eli Lilly's oral, once-daily GLP-1 receptor agonist, and the headline is that it is a small molecule, not a peptide, so it survives the gut and can be taken as a plain pill with no food or water restrictions. It is being developed for type 2 diabetes and obesity and has completed multiple successful Phase 3 trials. As of mid-2026 it is filed for regulatory review but not yet approved.

Weight Loss

CagriSema

Clinical Trials

CagriSema is a once-weekly injectable that pairs two drugs in one shot: semaglutide (a GLP-1 receptor agonist, the molecule behind Ozempic and Wegovy) and cagrilintide (a long-acting amylin analog). It is being developed by Novo Nordisk for obesity and type 2 diabetes, and in 2025 it cleared its phase 3 REDEFINE trials. It is not yet approved by the FDA, though regulatory filings are underway.

Weight Loss

Liraglutide

FDA

Liraglutide is a once-daily injectable GLP-1 receptor agonist, a synthetic peptide that shares about 97% of its sequence with the natural gut hormone GLP-1 but is engineered with a fatty acid chain so it survives in the body far longer. It is FDA-approved as Victoza for type 2 diabetes (2010) and as Saxenda for chronic weight management (2014), and is one of the most studied drugs in its class. As of 2024 a generic version is also FDA-approved.

Weight Loss

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