drugset / Trial / NCT07704892

A Study to Investigate Safety and Efficacy of Efimosfermin Compared With Placebo in Adult Participants With Compensated Cirrhosis Due to Metabolic Dysfunction-associated Steatohepatitis (MASH)

NCT07704892 ↗

Phase 3 Not yet recruiting 380 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a multi-center, randomized, two-part (Part A and Part B) study investigating the safety and efficacy of efimosfermin alfa in adult participants with compensated cirrhosis due to MASH. Participants who complete the treatment during Part A of the study and meet the inclusion criteria will have the option to enroll in Part B (open label) of the study.

Timeline

Start
2026-07-20
Primary completion
2030-10-14
Completion
2033-12-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Efimosfermin alfa Unknown — Subcutaneous