Preserved supervised synthesis

Survodutide synthesis · version 1

This URL preserves the exact reviewed public wording and source set for synthesis version 1.

Supervised synthesis

What do selected human studies report about Survodutide?

Manually reviewed August 19, 2026 · version 1

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A bounded review of two sponsor-funded randomized Phase 2 trials: one in obesity and one in metabolic dysfunction-associated steatohepatitis with fibrosis.12

Bottom line from this bounded source set

The reviewed obesity trial reported greater weight reduction than placebo, and the reviewed liver-disease trial reported more participants with improvement in steatohepatitis without worsening fibrosis. Both are mid-stage studies with substantial remaining uncertainty.12

Reviewed study record

Phase 2 obesity trial

Design

A randomized, double-blind, placebo-controlled dose-finding Phase 2 trial assessed body-weight change over 46 weeks.1

Population

The trial treated 386 adults with overweight or obesity without diabetes across 43 centers in 12 countries.1

Outcomes reported

Reported mean body-weight change ranged from -6.2% to -14.9% across planned survodutide groups and was -2.8% with placebo. About 60% completed the treatment period, and gastrointestinal events were more frequent with survodutide.1

Limitations

The sponsor-funded trial was Phase 2, had substantial treatment-period attrition, and Crossref registers a publisher erratum with two upstream dates for the same notice. Crossref metadata alone does not describe the corrected wording.1

Reviewed study record

Phase 2 MASH and fibrosis trial

Design

A randomized, placebo-controlled Phase 2 trial assessed histologic improvement in steatohepatitis without worsening fibrosis over 48 weeks.2

Population

The trial treated 293 adults with biopsy-confirmed metabolic dysfunction-associated steatohepatitis and fibrosis stages F1 through F3.2

Outcomes reported

Improvement in steatohepatitis without worsening fibrosis was reported in 43% to 62% across survodutide groups and 14% with placebo. Improvement in fibrosis by at least one stage was reported in 34% to 36% and 22%, respectively.2

Limitations

The sponsor-funded, 48-week Phase 2 trial was not designed to establish long-term liver-related clinical outcomes or uncommon harms, and the fibrosis result was a secondary endpoint.2

Reviewed source set

  1. PubMed · 38330987Glucagon and GLP-1 receptor dual agonist survodutide for obesity: a randomised, double-blind, placebo-controlled, dose-finding phase 2 trial ↗PubMed PMID 38330987 · EFetch XML reviewed 2026-08-19 · payload SHA-256 708a8ad3d65324a07e1f430e5b7710593929f992f466051274b69eb0fd4b1a47
    Publication update registered by CrossrefErratum ↗ · publisher metadata · December 17, 2025 and February 1, 2026. Crossref metadata identifies the notice but does not by itself explain what wording changed.
  2. PubMed · 38847460A Phase 2 Randomized Trial of Survodutide in MASH and Fibrosis ↗PubMed PMID 38847460 · EFetch XML reviewed 2026-08-19 · payload SHA-256 7f3ce949e27c7ac79fc7f5dd37e709d2fea19edd0b0b04b599c4d49e4b6b1093
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1056/nejmoa2401755. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗