A Phase 2 interventional study of Resmetirom and Placebo Control in MASLD - Metabolic Dysfunction-Associated Steatotic Liver Disease and HIV (Human Immunodeficiency Virus), sponsored by Naga P. Chalasani. Recruiting at 10 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-30.
Sponsored by Naga P. Chalasani · Phase 2, Interventional, and Treatment
The purpose of this research study is to test the safety and effectiveness of the study drug, resmetirom, in participants with MASLD and HIV. This is a research study to test a drug that is already on the market with a population that was not included in the original clinical trials. Participants will be people over age 18 with HIV who are on antiretroviral therapy and have been diagnosed with MASLD.
Researchers will compare resmetirom to placebo (a look-alike substance that contains no drug) to see if resmetirom decreases the amount of fat in the liver.
Participants will:
2,041 studies on the registry are indexed under Acquired Immunodeficiency Syndrome; 272 are open to participants now.
This study's planned enrollment of 120 is above the median of 105 across 1,543 interventional studies indexed under Acquired Immunodeficiency Syndrome.
Browse Acquired Immunodeficiency Syndrome studies →Naga P. Chalasani is the lead sponsor of 3 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Any of the following laboratory values at screening:
Resmetirom - 80mg or 100mg based on participant weight
Drug: Resmetirom
Placebo
Drug: Placebo Control
Resmetirom - 80mg or 100mg based on participant weight
Placebo - an identical looking tablet with no medicinal properties
Change from baseline in hepatic fat content at week 24
Time frame: From baseline to the end of treatment at 24 weeks
Proportion of participants with reduction of at least 30% in hepatic fat content from baseline to week 24
Time frame: Baseline to the end of treatment at week 24
Change from baseline in liver enzyme parameters, lipid profile and fasting glucose
Time frame: From baseline to end of treatment at week 24
Plan to share: Undecided — Await IRB determination of privacy and HIPAA issues
No publications or documents are linked to this record.
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
Contact study teamGet an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Acquired Immunodeficiency Syndrome→
Naga P. Chalasani