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Approved In China

Mazdutide

Also known as IBI362 · LY3305677

Summary coverage

At a glance

What it is
Glucagon/GLP-1 dual agonist approved in China, not by FDA.
Evidence
Clinical trialsHow the tiers workGLORY-2 (JAMA, 7 June 2026, NCT06164873, n=461 across 27 Chinese hospitals) reported −16.65% against −1.50% on placebo at 60 weeks on 9 mg weekly, with 84.3% against 33.1% reaching at least 5% loss. Why this tier
Half-life
About 6 to 17 days in early trials, varying widely from person to person
From Phase 1b trials, PubMed 34430840 and 35750681
Routes
Subcutaneous
Category
Metabolic
FDA
Investigational
As of 3 August 2026. What that means
WADA
We do not state a status

Putting Mazdutide on a schedule, with the vial it comes from and a log of each dose, happens in the app: Claritide for iPhone.

Evidence

Why this tier

GLORY-2 (JAMA, 7 June 2026, NCT06164873, n=461 across 27 Chinese hospitals) reported −16.65% against −1.50% on placebo at 60 weeks on 9 mg weekly, with 84.3% against 33.1% reaching at least 5% loss. In the earlier GLORY-1 trial, the 4 mg and 6 mg arms gave −11.00% and −14.01% at 48 weeks against +0.30% on placebo on the treatment-policy estimand (NEJM); Innovent’s headline figures, −12.05% and −14.84%, are the efficacy estimand. The caveat is the population: Chinese adults, with a lower baseline BMI and a younger mean age (33.9 years) than Western obesity trials, so the generalisability of the effect size to a different population is genuinely uncertain.

Overview

What it is

Mazdutide is a glucagon and GLP-1 dual agonist that originated at Eli Lilly and is licensed to Innovent. China approved it for chronic weight management in June 2025 and later for glycaemic control in type 2 diabetes. It is not FDA-approved. Its pivotal data comes from Chinese adults, a population with a lower baseline BMI and a younger mean age than Western trials, which is the caveat that makes the record worth carrying.

Mechanism

How it works

The same dual mechanism as survodutide: GLP-1 receptor agonism for appetite suppression, slowed gastric emptying and glucose-dependent insulin release, plus glucagon receptor agonism for increased energy expenditure and hepatic fat oxidation, with the GLP-1 arm offsetting glucagon’s effect on blood sugar.

Dosing

Commonly researched ranges

These are figures reported in published literature and practitioner protocols: a commonly researched range, not a recommendation. Claritide does not tell you what to take.
  • GLORY-1 Phase 3 doses · the two approved strengths4–6 mg

    Once weekly for 48 weeks

    Both arms of GLORY-1, and both approved by China’s NMPA for chronic weight management on 27 June 2025. Stated first because the record previously showed only the 9 mg dose, which is the one that is not approved anywhere.

  • GLORY-2 Phase 3 dose9 mg

    Once weekly for 60 weeks

    The dose in GLORY-2 (NCT06164873). Its supplementary application was accepted for NMPA review in November 2025, and we found no approval as of 27 September 2026; nothing about mazdutide is approved in the US or the EU.

Cycle guidance
Not established in available literature
Goals
Fat loss
Legal standing

Where this sits with the FDA

Dated, sourced, and separate from whether it works. Removal from a warning list is not permission to compound.
Investigationalas of 3 August 2026 · US

Approved by China’s NMPA and not by FDA. An approval in one jurisdiction is a real regulatory event and it does not make a product lawful, labelled or supply-chain-verified in another.

Last change · 1 June 2025 · China’s National Medical Products Administration approved mazdutide for chronic weight management in June 2025; our source does not give an exact day.

Primary source
Sport

WADA status

The 2026 Prohibited List entered force on 1 January 2026.
We do not state a status

Not named on the 2026 Prohibited List. We could not determine a classification and do not state one.

We looked and could not resolve it. This is not the same as "not prohibited". Treat it as unresolved and check with your federation before competing.

Reconstitution

Mixing recipes our sources document

Concentration (mg/mL) = vial mg ÷ diluent mL. On a U-100 barrel, 1 unit = 0.01 mL.

Not established in available literature. Use the calculator with the figures printed on your own vial.
Open the calculator

Expectations

Week by week

What our material describes people reporting. Individual responses vary widely.

Not established in available literature.

Tolerability

Side effects

Grouped by how often our sources report them. Percentages appear only where a published trial figure exists.

Common

  • Vomiting53.1% in trialsGLORY-2, 9 mg arm.
  • Nausea46.9% in trialsGLORY-2, 9 mg arm.
  • Diarrhoea39.4% in trialsGLORY-2, 9 mg arm.

Uncommon

  • Discontinuation for adverse events2.9% in trials2.9% against 0% on placebo, a low discontinuation rate given the GI numbers above.
Safety

Contraindications and interactions

Do not use if

Not established in available literature.

Interactions

Not established in available literature.

Absence from this list does NOT mean safety. It means lack of research.

Handling

Storage and cost

Storage
Our sources publish no reconstitution or storage protocol for mazdutide.
Cost
Not established in available literature
Deep dive

Mazdutide in full

Limited coverage

Mazdutide is a glucagon and GLP-1 dual agonist, originated at Eli Lilly and licensed to Innovent. Once weekly, subcutaneous. Approved by China's National Medical Products Administration for chronic weight management in June 2025, and later for glycaemic control in type 2 diabetes. Not FDA-approved.

The data

GLORY-2, published in JAMA on 7 June 2026: NCT06164873, 461 participants across 27 Chinese hospitals, 9 mg weekly for 60 weeks. Weight change −16.65% against −1.50% on placebo, with 84.3% against 33.1% reaching at least 5% loss. Discontinuation for adverse events was 2.9% against 0%.

Gastrointestinal effects were substantial: vomiting 53.1%, nausea 46.9%, diarrhoea 39.4%.

In the earlier GLORY-1 trial, the 4 mg and 6 mg arms gave −11.00% and −14.01% at 48 weeks against +0.30% on placebo, on the treatment-policy estimand published in NEJM. Innovent’s headline figures for the same arms, −12.05% and −14.84%, are the efficacy estimand: the same trial, a different question.

The caveat that is the point

The pivotal data comes from Chinese adults, a population with a lower baseline BMI and a younger mean age than Western obesity trials, at 33.9 years.

That is not a criticism of the trial. It is a statement about what the number transfers to. Percentage weight loss is not obviously portable across populations with different starting body composition, different baseline metabolic disease burden and different average age. A 16.65% result in a 34-year-old cohort with a lower starting BMI is a different fact from a 16.65% result in a 50-year-old Western cohort, and it is the kind of distinction that disappears entirely when a number is copied into a comparison table.

Mazdutide is being sold into the US on the strength of that number.

References

Sources

  1. 1
    JAMA, 7 June 2026 · GLORY-2, mazdutide 9 mg weekly for 60 weeks, n=461
  2. 2
    ClinicalTrials.gov NCT06164873 · GLORY-2 (CIBI362B302), Innovent (record last updated August 2024; read 27 September 2026)
  3. 3
    Innovent · mazdutide receives NMPA approval for chronic weight management
  4. 4
    Innovent, 25 May 2025 · GLORY-1 published in NEJM: the 4 mg and 6 mg arms, with both estimands (dose review, 2026-08-17; read 27 September 2026)
  5. 5
    Ji et al., NEJM, 25 May 2025 · GLORY-1, mazdutide 4 mg and 6 mg for 48 weeks, n=610, treatment-policy estimand
  6. 6
    Innovent, 25 November 2025 · the mazdutide 9 mg supplementary application accepted for NMPA review, i.e. not approved; no approval found as of 27 September 2026

Every record in this library is free to read, and it stays free. Your own schedule, vials and log live in the app: Claritide for iPhone.