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MetabolicResearch strength: ModerateEvidence: Moderate

Survodutide

Survodutide (GLP-1 / glucagon dual agonist)

An investigational once-weekly GLP-1 and glucagon receptor dual agonist studied for obesity and metabolic liver disease.

Overview

Survodutide is an investigational dual agonist of the GLP-1 and glucagon receptors developed for obesity and metabolic dysfunction-associated steatohepatitis (MASH). The glucagon component adds energy expenditure and liver-directed effects to the appetite and glucose benefits of GLP-1. Phase 2 trials reported meaningful weight loss and improvement in liver disease. It is not yet approved.

Mechanism of action

Agonizes both GLP-1 and glucagon receptors, combining appetite suppression and improved glucose handling with increased energy expenditure and hepatic fat reduction.

Key studies & citations

  • Human2024

    A Phase 2 randomized trial of survodutide in MASH and fibrosis

    48-week trial in 293 adults with biopsy-confirmed MASH: histologic improvement without worsening fibrosis in 47 to 62% on survodutide versus 14% on placebo.

    New England Journal of Medicine
  • Human2024

    Glucagon and GLP-1 receptor dual agonist survodutide for obesity: a randomised, double-blind, placebo-controlled, dose-finding phase 2 trial

    46-week trial in 387 adults without diabetes: mean weight change of minus 14.9% at 4.8 mg weekly versus minus 2.8% on placebo; gastrointestinal adverse events were common.

    The Lancet Diabetes and Endocrinology
  • Human2026

    Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial

    Phase 3 in 216 adults: 84% on survodutide 6 mg versus 24% on placebo achieved at least a 30% liver-fat reduction, with minus 12.2% versus minus 1.0% body weight at 48 weeks.

    Nature Medicine

Frequently asked questions

How is survodutide different from tirzepatide?

Both are dual agonists, but survodutide targets GLP-1 and glucagon receptors, while tirzepatide targets GLP-1 and GIP. The glucagon component is being studied especially for liver fat.

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