Preserved supervised synthesis

Survodutide synthesis · version 2

This URL preserves the exact reviewed public wording and source set for synthesis version 2.

Supervised synthesis

What do selected human studies report about Survodutide?

Manually reviewed September 15, 2026 · version 2

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Four selected phase 2 and phase 3 reports examine survodutide in obesity and liver disease. Weight, MRI liver-fat and histological endpoints are different outcomes and should not be treated as interchangeable.1234

Bottom line from this bounded source set

Selected studies reported improvements in weight or liver-related measurements. The newer phase 3 reports also found frequent gastrointestinal adverse events. These measured changes do not establish every long-term clinical benefit, and linked correction notices remain relevant to interpretation.1234

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 study record

SYNCHRONIZE-1: phase 3 obesity study

Design

A blinded randomized placebo-controlled trial assessed percentage weight change and at least 5% weight reduction at 76 weeks, under NCT06066515.3

Population

The report describes 725 adults with obesity or overweight with a related complication, excluding diabetes.3

Outcomes reported

The treatment-regimen analysis reported mean weight changes of −12.2% and −13.0% in the active groups versus −5.4% with placebo. Gastrointestinal events occurred in 80.9% and 89.7% of active groups versus 47.9% with placebo.3

Limitations

The analysis includes treatment discontinuation and other specified intercurrent events. Weight reduction does not itself establish fewer cardiovascular events or other long-term complications. No deaths were reported.3

Reviewed study record

SYNCHRONIZE-MASLD: liver-fat and weight endpoints

Design

A blinded randomized placebo-controlled phase 3 study assessed MRI-measured liver-fat reduction and weight change at 48 weeks.4

Population

The abstract describes 216 treated adults with obesity and at-risk metabolic dysfunction-associated steatotic liver disease.4

Outcomes reported

Under the treatment-regimen analysis, 68.5% with survodutide and 28.6% with placebo reached at least 30% liver-fat reduction. Mean weight changes were −8.7% and −1.4%, respectively. Gastrointestinal adverse events were common.4

Limitations

The larger estimates in the efficacy analysis answer a different question from the treatment-regimen analysis. MRI liver fat is not a clinical liver-event outcome. A linked publisher correction is recorded with this source; follow-up was short and recruitment was limited to the United States and Spain.4

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 ↗
  3. PubMed · 42253238Survodutide Once Weekly for the Treatment of Adults with Obesity. ↗PubMed PMID 42253238 · EFetch XML reviewed 2026-09-15 · payload SHA-256 af8146d991ea6927b0e5f817c6ba5c66af5c5b9047dcafda697686a950bddc74
    No registered Crossref update in the reviewed snapshotChecked September 15, 2026 for DOI 10.1056/nejmoa2600751. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗
  4. PubMed · 42252333Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial. ↗PubMed PMID 42252333 · EFetch XML reviewed 2026-09-15 · payload SHA-256 8ff54e61f7e5c23301b3c5ba7985aae0ffb2aace1063e036f079a7134a1d8432
    Publication update registered by CrossrefCorrection ↗ · publisher metadata · August 25, 2026. Crossref metadata identifies the notice but does not by itself explain what wording changed.