- A Study to Investigate the Safety and Efficacy of GSK4532990 Compared With Placebo in Adult Participants Aged 18 to 70 Years With Alcohol-related Liver Disease — Recruiting • Phase II • Gastroenterology • NCT06613698.
- The goal of this study is to assess the safety and efficacy of GSK4532990 in participants with alcohol-related liver disease.
- Sponsor: GlaxoSmithKline.
Verify eligibility, endpoints and current status on the original source registry before acting on this summary.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
The goal of this study is to assess the safety and efficacy of GSK4532990 in participants with alcohol-related liver disease.
- : * Capable of giving signed informed consent prior to the performance of any study-specific procedures. * Able and willing to comply with all study assessments and adhere to the protocol schedule of activities. * In the opinion of the investigator, there is a history of alcohol consumption compatible with either ALD or Met ALD. * A female participant is eligible to participate after meeting additional pre-defined criteria. * Participants must meet predefined stable use requirements of concomitant medications based on study criteria. * Participant has advanced chronic liver disease
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.