Survodutide
Metabolic Health · GLP-1/glucagon agonist (dual)
Tier B
Bottom line
Read Off Label grades Survodutide as B (6.8/10) based on strong evidence, high benefit magnitude, and a med-risk safety profile.
Boehringer Ingelheim/Zealand Pharma.
Studied, labeled, or reported-use context: 3. — Investigational; not individualized guidance.
What the evidence says
Boehringer Ingelheim/Zealand Pharma. SYNCHRONIZE-1 (no T2D) Phase 3 full results published in NEJM (Jun 2026, ADA Scientific Sessions): -16.6% mean body weight at 76 weeks vs -3.2% placebo (efficacy estimand), 85% achieving >=5% loss, loss driven predominantly by fat mass. SYNCHRONIZE-MASLD (Nature Medicine, Jun 8 2026; n=218, obesity + MASLD): met co-primary endpoints (>=30% MRI-PDFF liver-fat reduction and % body-weight change at 48 wk) -- 6 in 10 participants reached liver-fat normalization, the first dedicated MASLD Phase 3 readout for the class. SYNCHRONIZE-2 (with T2D, n=752) and the CVOT remain ongoing. Phase 2 (Le Roux 2024 Lancet) showed up to 19% weight loss.
Mechanism
Dual GLP-1 receptor and glucagon receptor agonist; glucagon arm increases energy expenditure and hepatic fat oxidation; particular interest for MASLD/metabolic liver disease
Studied, labeled, or reported dose & route
3.6 or 6.0 mg SC weekly (Phase 3 doses); titrated
This records doses and routes described in studies, approved labeling, clinical practice, or documented use. It is not individualized guidance and does not establish safety; context changes with indication, formulation, health history, monitoring, and other medicines.
Citations
- DOI · 10.1111/dom.70196
- DOI · 10.1111/dom.70263
- DOI · 10.1016/j.conctc.2026.101611
- DOI · 10.1186/s12933-026-03140-0
- DOI · 10.1007/s11695-026-08692-4
- DOI · 10.3390/livers6030035
- nature.com
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Common questions
- What does the evidence show about Survodutide's effects?
- Read Off Label rates the evidence for Survodutide as Strong and the benefit magnitude as high, producing an overall grade of B (6.8/10). Boehringer Ingelheim/Zealand Pharma.
- What safety findings are reported for Survodutide?
- Survodutide has a med risk profile in the database. Med (similar GI profile to GLP-1 class; no unexpected signals to date) Legal status: Investigational (Phase 3).
- What doses or routes are reported for Survodutide?
- 3.6 or 6.0 mg SC weekly (Phase 3 doses); titrated This is context from studies, approved labeling, clinical practice, or documented use; it is not individualized guidance and does not establish safety.
- How does Survodutide work?
- Dual GLP-1 receptor and glucagon receptor agonist; glucagon arm increases energy expenditure and hepatic fat oxidation; particular interest for MASLD/metabolic liver disease
This is an independent synthesis of published research by a non-clinician. Scores are opinions supported by citations, not prescriptions. See the full disclaimer and methodology for how this score was produced and what it does and doesn't mean.