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Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Trial abstract

SURVO-PH2-MASH — structured trial abstract

SURVO-PH2-MASH — Survodutide in mash: randomised, double-blind, placebo-controlled

Document identifier
CEI-TR-0057
Series
Trial abstract
Version
2.4
Published
08 Jan 2024
Last reviewed
08 Dec 2024
Next review
08 Dec 2026
Identifier
10.71829/cei.trial.57
Certainty
Low
Cycle
2024 Q1
Phase
Phase 2
Status
Reported

§1Structured abstract

§1.1Objective

To evaluate Survodutide in metabolic dysfunction-associated steatohepatitis, against the comparator specified in §2, with the primary endpoint stated below.

§1.2Design

Design
Randomised, double-blind, placebo-controlled, parallel-group
Masking
Double-blind (participant, investigator and sponsor)
Phase
Phase 2
Randomised participants
295
Duration of the primary analysis period
48 weeks
Sponsor class
Manufacturer-sponsored
Registry identifier
not reproduced — see the note in §1.5

§1.3Primary endpoint

Histological improvement in metabolic dysfunction-associated steatohepatitis without worsening of fibrosis

§1.4Principal result

Improvement in 62 % to 83 % across doses versus 18 % with placebo.

§1.5Provenance of this abstract

Table 1. Field-by-field provenance. The Institute records which fields are extracted from a source and which are its own reconstruction, so that a reader can tell the two apart without leaving the page.

FieldProvenanceNote
Design, phase, duration, primary endpointExtractedReproduced from the published report or the registry record.
Randomised participantsExtractedReproduced as published.
Principal resultExtractedReproduced as published, with the confidence interval where the Institute holds it.
Centres, countries and baseline characteristicsReconstructedDerived by the Institute from the design class and the randomised total. Presented in §2 as an illustrative operational profile and marked as such. These figures are not published characteristics of this trial.
Certainty assessmentInstitute judgementThe Institute’s own domain-by-domain assessment, with reasoning recorded against each domain in §4.
Registry identifierNot heldThe Institute does not reproduce a registry identifier it has not verified and never constructs one. Documents are referenced by the Institute’s own identifier.
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