For research and educational purposes only. Not medical advice.
Mazdutide Reference
Educational, not medical advice reference for Mazdutide: GLP-1, Fat Loss; regulatory status, evidence posture, source review, and schedule notes…
Reference summary
GLORY-1 (Ji 2025 NEJM, Phase 3, Chinese adults with obesity or overweight, 48 weeks) reported clinically meaningful placebo-subtracted weight reductions at both the 4 mg and 6 mg once-weekly doses, in the range typically reported for GLP-1 / glucagon dual agonists in similar populations. Adverse events were predominantly gastrointestinal (nausea, diarrhea, vomiting), dose-dependent, with most events graded mild to moderate. The trial was conducted in a Chinese population and the Phase 3 program outside of China is at earlier stages.
Regulatory and posture
- Categories
- GLP-1, Fat Loss
- Aliases
- IBI362, LY3305677, GLP-1 / glucagon dual receptor agonist
- Evidence posture
- human - Phase 3 data exist in a Chinese population. Approved in China 2025; investigational outside China.
- Regulatory status
- Investigational in the United States. Mazdutide is Innovent Biologics' GLP-1 / glucagon dual receptor agonist (originally licensed from Eli Lilly). China's NMPA approved mazdutide in 2025 for adults with obesity or overweight (the first dual-agonist approval in China for this indication). There is no FDA-approved drug label in the US or EU, and mazdutide is not on FDA's approved bulk-substances list for compounding.
- Content review status
- investigational verified
Selected public sources
- ClinicalTrials.gov Phase 3 mazdutide (IBI362) GLORY program search
- PubMed: Ji et al. N Engl J Med 2025 - once-weekly mazdutide in Chinese adults with obesity or overweight (Phase 3) (PMID 40421736)
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