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Reporter brief

The Effect of Semaglutide in Subjects With Non-cirrhotic Non-alcoholic Steatohepatitis

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Trial registry update: ACTIVE_NOT_RECRUITING. No results reported in the supplied registry record.

Assessment pending; this report does not establish a change in evidence.

  • This abstract contains no results, only study design details, so no efficacy claims can be assessed.
  • The study is still ongoing (described prospectively), so outcomes remain unknown.
  • No information is provided on which specific NASH endpoints (fibrosis, inflammation, liver function, or clinical events) will be measured or have been achieved.

Rct; Human.

Subjects with non-cirrhotic non-alcoholic steatohepatitis (NASH). Excludes participants with other chronic liver diseases. Excludes pregnant, breast-feeding, or potentially pregnant women.

Design
Rct
Sample
—
Journal
Novo Nordisk A/S
Published
Sep 4, 2026

Not recorded.

  • Assessment: Unassessed.
  • Only the source material recorded on this evidence page was assessed.

Novo Nordisk A/S (sponsor) · Study is conducted by Novo Nordisk A/S, the manufacturer of semaglutide

See the GLP-1 agonists timeline and recorded assessment for prior evidence.

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