What the studies show
Phase 2 in 293 patients: MASH improvement without worsening fibrosis in 83% at 4.8 mg versus 18% on placebo at 48 weeks; fibrosis improvement in 52% versus 26%. Phase 3 LIVERAGE ongoing.
Human trials exist and mostly agree, but there are too few of them, they are too small, or one big one is still reading out. Expect the grade to move.
- 1Sanyal AJ, et al. A phase 2 randomized trial of survodutide in MASH and fibrosis.N Engl J Med, 2024; DOI 10.1056/NEJMoa2401755293 patients, 48 weeks.
In context
Survodutide is a once-weekly peptide that activates both the GLP-1 and glucagon receptors. In SYNCHRONIZE-1, a 725-person phase 3 trial published in June 2026, it produced 12–13% weight loss at 76 weeks against 5% on placebo, with gastrointestinal symptoms in up to 90% of participants. Its distinctive result is in the liver: a phase 2 trial resolved MASH without worsening fibrosis in 83% of patients at the top dose. It is not approved anywhere.
Survodutide is investigational. Legal status differs by country — see the regulation section or the jurisdiction pages.
Questions
Is Survodutide proven to help with liver disease?
What studies are behind the grade?
Is Survodutide approved for this?
Other outcomes for Survodutide
- BBody weight1 phase 3 RCT + phase 2
- BLiver fat and visceral fatPhase 3 (SYNCHRONIZE-MASLD)
- BGI side effectsadversePhase 3
- BHeart rate increaseadversePhase 2 + 3
Reviewed 3 September 2026. Grades count human evidence only; see how LYO grades. Not medical advice. Correct this page →