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Clinical Trials in the EU / 2026-526391-23-00
Authorised, not yet recruiting Phase II

A Dose-finding, Double-blind, Randomized, Placebo-controlled Phase 2 Study to Evaluate the Efficacy and Safety of Treatment with Efimosfermin Alfa in Adult Participants with Alcohol-related Liver Disease (ALD)

2026-526391-23-00 · tracked via the Priya Life Science EU tracker
Sponsor
Glaxosmithkline Research & Development Limited
Sponsor type
Pharmaceutical company
Therapeutic area
Digestive System Diseases
Decision date
12/10/2026
Enrollment target
97
Sites
Spain, Denmark, Italy, Poland, France, Germany, Greece

Condition studied

Liver Diseases, Alcoholic

Investigational medicinal product(s)

Placebo for efimosfermin powder for solution for injection

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

Change from baseline in VCTE-LSM using FibroScan, Dual endpoints: • Change from baseline in VCTE-LSM using FibroScan • Change from baseline in MELD

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-526391-23-00 on CTIS ↗ ← All trials in the EU