Catalog classification, reference sizes, lab math links, and source-backed data. Educational use only — not medical advice.
Researched for: Survodutide evidence and protocol review
Also known as: BI 456906
Survodutide is a glucagon/GLP-1 receptor dual agonist. The Phase 3 SYNCHRONIZE-1 trial (NEJM, presented at ADA 2026; N=725) reported up to 16.6% mean weight loss at 76 weeks versus 3.2% placebo, with up to 85.1% of participants achieving >=5% weight reduction. Pre-specified body-composition analysis reported up to 34% visceral fat reduction and up to 63.1% liver fat reduction, with lean-mass loss limited to <=10.8% of total tissue-mass change at the highest dose. Not yet FDA-approved as of 2026.
Catalog descriptions reflect research context only. Not a medical claim or treatment recommendation.
Data source: Primary literature, regulator records, trial registries, and identity-specific evidence search
Reflects preclinical/research literature context only. Not a medical claim, dosing instruction, or treatment recommendation.
Survodutide remains investigational. The Phase 2 obesity study used different arm-specific 20-week escalations and permitted tolerability-driven adjustment during the flexible phase; one generic ladder would be inaccurate.
Supplementary research context only. Not medical advice or a treatment recommendation.
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Published articles on this site that mention Survodutide or one of its catalog aliases.
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Research Use Only. All content is for educational and research reference only. Not medical advice, a treatment recommendation, or guidance on human use. Compounds are not FDA-approved drugs unless specifically noted.