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Active Not RecruitingNCT05583344

Phase 2b Study of GSK4532990 in Adults With NASH

17 β-Hydroxysteroid Dehydrogenase Type 13 Minimization for the Treatment of NASH (HORIZON): A Double-Blind, Placebo-Controlled Phase 2b Study to Evaluate the Efficacy and Safety of GSK4532990 in Adults With Nonalcoholic Steatohepatitis

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
284 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to measure improvements in liver fibrosis and inflammation with GSK4532990 compared with placebo in participants with NASH and advanced fibrosis on biopsy (F3 or F4). The study duration will be up to 76 weeks including the screening period. The treatment duration will be up to 52 weeks.

Conditions

Interventions

TypeNameDescription
DRUGGSK4532990GSK4532990 will be administered.
DRUGPlaceboPlacebo will be administered.

Timeline

Start date
2023-01-02
Primary completion
2026-01-31
Completion
2027-04-05
First posted
2022-10-17
Last updated
2026-03-24

Locations

170 sites across 17 countries: United States, Argentina, Australia, Belgium, Canada, France, Greece, India, Italy, Japan, Mexico, Panama, Puerto Rico, South Korea, Spain, Turkey (Türkiye), United Kingdom

Regulatory

Source: ClinicalTrials.gov record NCT05583344. Inclusion in this directory is not an endorsement.