Back to Search Start Over

Semaglutide 2.4 mg in Participants With Metabolic Dysfunction‐Associated Steatohepatitis: Baseline Characteristics and Design of the Phase 3 ESSENCE Trial.

Authors :
Newsome, Philip N.
Sanyal, Arun J.
Engebretsen, Kristiane A.
Kliers, Iris
Østergaard, Laura
Vanni, Denise
Bugianesi, Elisabetta
Rinella, Mary E.
Roden, Michael
Ratziu, Vlad
Source :
Alimentary Pharmacology & Therapeutics. Dec2024, Vol. 60 Issue 11/12, p1525-1533. 9p.
Publication Year :
2024

Abstract

Background: Semaglutide, a glucagon‐like peptide‐1 receptor agonist, has demonstrated potential beneficial effects in metabolic dysfunction‐associated steatohepatitis (MASH). Aims: To describe the trial design and baseline characteristics of the 'Effect of Semaglutide in Subjects with Non‐cirrhotic Non‐alcoholic Steatohepatitis' (ESSENCE) trial (NCT04822181). Methods: ESSENCE is a two‐part, phase 3, randomised, multicentre trial evaluating the effect of subcutaneous semaglutide 2.4 mg in participants with biopsy‐proven MASH and fibrosis stage 2 or 3. The primary objective of Part 1 is to demonstrate that semaglutide improves liver histology compared with placebo. The two primary endpoints are: resolution of steatohepatitis and no worsening of liver fibrosis, and improvement in liver fibrosis and no worsening of steatohepatitis. The Part 2 objective is based on clinical outcomes. The current work reports baseline characteristics of the first 800 randomised participants which includes demographics, laboratory parameters, liver histology, non‐invasive tests and presence of metabolic dysfunction‐associated steatotic liver disease (MASLD) cardiometabolic criteria. Results: Of 800 participants, 250 (31.3%) had fibrosis stage 2 and 550 (68.8%) had fibrosis stage 3. In the overall population, mean (standard deviation [SD]) age was 56 (11.6) years, 57.1% were female, mean (SD) body mass index was 34.6 (7.2) kg/m2, 55.5% had type 2 diabetes and > 99% had at least one MASLD cardiometabolic criterion according to the published definition. Conclusion: The ESSENCE baseline population includes participants with clinically significant fibrosis stages 2 and 3. Although MASLD cardiometabolic criteria were not a requirement for study enrolment, almost all participants (> 99%) had at least one MASLD cardiometabolic criterion. Trial Registration: NCT04822181 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02692813
Volume :
60
Issue :
11/12
Database :
Academic Search Index
Journal :
Alimentary Pharmacology & Therapeutics
Publication Type :
Academic Journal
Accession number :
181154968
Full Text :
https://doi.org/10.1111/apt.18331