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RecruitingNCT07143968Updated Jul 30, 2026

A Study to Evaluate the Use of Resmetirom in Participants With MASLD and HIV

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

From the registry’s dates

  • Started Apr 2026; still recruiting 5 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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:

  • Complete 3 screening visits to determine eligibility.
  • Take resmetirom or placebo every day for 24 weeks if eligible.
  • Have 2 MRI scans to measure the amount of fat on the liver. One will be before treatment starts and one will be at the end of 24 weeks of treatment.
  • Attend 3 scheduled clinic visits while on treatment for bloodwork and safety assessments.
  • Participate in 3 phone calls while on treatment and one phone call 4 weeks after treatment is completed to check for safety and any health changes.
02

Conditions studied

  • MASLD - Metabolic Dysfunction-Associated Steatotic Liver Disease
  • HIV (Human Immunodeficiency Virus)
03

In context

Acquired Immunodeficiency Syndrome

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Adults (≥18 years of age) with documented HIV.
  2. Documented diagnosis of MASLD established by imaging (ultrasound, CT scan or MRI) or vibration-controlled transient elastography (VCTE) or liver biopsy within 12 months before screening.
  3. Hepatic fat fraction ≥8% by MRI-PDFF.
  4. Liver stiffness by VCTE ≥8 kPa and CAP≥263 dB/m
  5. HIV-1 RNA \<200 copies/mL for ≥6 months on antiretroviral therapy (ART) (must have screening HIV-1 RNA value and one clinical care value within 6 months prior to screening and up to the randomization that meet the criteria).
  6. Stable ART regimen for ≥3 months prior to screening and stable up to the randomization and no active plans to change ART while on study.
  7. Willingness to participate in the study.

Exclusion criteria

Exclusion Criteria:

  1. History of significant alcohol consumption (defined as >2 drinks/day on average for men, >1 drinks/day on average for women) for at least 3 consecutive months (12 consecutive weeks) within 5 year before screening
  2. History of other acute or chronic liver disease, including, but not limited to autoimmune, primary biliary cholangitis, Wilson's disease, alpha 1 antitrypsin deficiency, hemochromatosis, hepatitis B virus (HBV), and ongoing or recent (within the past 3 years) hepatitis C RNA positivity.
  3. History of liver transplant.
  4. Liver biopsy or radiologic imaging consistent with the clinical presence of cirrhosis or portal hypertension at screening.
  5. Participants whose Visit 2 ALT, AST, or alkaline phosphatase (ALP) values exceed their Visit 1 values by more than 50%.
  6. Inability to undergo MRI testing
  7. Uncontrolled T2DM defined as glycated hemoglobin (HbA1c) >9.5% at screening.
  8. Any of the following laboratory values at screening:

    1. ALT or AST >250 U/L.
    2. Total bilirubin (TBL) >1.5 mg/dL and direct bilirubin > 0.5 mg/dL (unless due to Gilbert's disease or atazanavir use, per the opinion of the site investigator).
    3. Platelet count \<150,000/mm3.
    4. Estimated glomerular filtration rate (e-GFR) \<60 mL/min/1.73m2 using the chronic kidney disease-epidemiology collaboration (CKD-EPI) equation
    5. International normalized ratio (INR) >1.3.
    6. Albumin \< 3.6 g/dL
  9. Liver stiffness measurement (LSM) by VCTE > 20 kPa
  10. Further exclusion criteria apply
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Treatment

    Resmetirom - 80mg or 100mg based on participant weight

    Drug: Resmetirom

  • Placebo comparator
    Placebo

    Placebo

    Drug: Placebo Control

Interventions

  • DrugResmetirom

    Resmetirom - 80mg or 100mg based on participant weight

  • DrugPlacebo Control

    Placebo - an identical looking tablet with no medicinal properties

06

What researchers measure

Primary outcomes

  1. Change from baseline in hepatic fat content at week 24

    Time frame: From baseline to the end of treatment at 24 weeks

Secondary outcomes

  1. 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

  2. Change from baseline in liver enzyme parameters, lipid profile and fasting glucose

    Time frame: From baseline to end of treatment at week 24

07

Study locations

5 of 10 sites recruiting
  • University of Alabama Birmingham
    Birmingham, Alabama 35294, United States
    • Kristen Spraggins · Contact · kspraggins@uabmc.edu · 205-934-9346
    • Sonya Heath, MD · Principal investigator
    Recruiting
  • UC San Diego Altman Clinical and Translational Research Institute
    La Jolla, California 92037, United States
    Not yet recruiting
  • University of California, San Francisco
    San Francisco, California 94143, United States
    Not yet recruiting
  • Atlantic Clinical Research Institute
    West Palm Beach, Florida 33409, United States
    • Amanda Chavez · Contact · achavez@midwaycare.org · 561-249-2279
    • Hector Bolivar, MD · Principal investigator
    Recruiting
  • Indiana University
    Indianapolis, Indiana 46202, United States
    • Lexi Smith · Contact · agoy@iu.edu · 317-278-0697
    • Samer Gawrieh, MD · Principal investigator
    Recruiting
  • Johns Hopkins University
    Baltimore, Maryland 21205, United States
    • Sara Mekhael · Contact · sawad3@jhu.edu · 410-550-3015
    • Mark Sulkowski, MD · Principal investigator
    Recruiting
  • Mt Sinai Health System
    New York, New York 10029, United States
    • Mark Miller · Contact · mark.miller@mssm.edu · 212-824-7672
    • Meena Bansal, MD · Principal investigator
    Not yet recruiting
  • Duke University Medical Center
    Durham, North Carolina 27710, United States
    Not yet recruiting
  • UT Health Houston
    Houston, Texas 77030, United States
    Recruiting
  • Virginia Commonwealth University
    Richmond, Virginia 23298, United States
    Not yet recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — Await IRB determination of privacy and HIPAA issues

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07143968
Lead sponsor
Naga P. Chalasani
Responsible party
Naga P. Chalasani (Professor of Medicine, Indiana University) — Sponsor-investigator
First posted
Aug 27, 2025
Start date
Apr 23, 2026
Primary completion
Oct 2027 (estimated)
Completion
Nov 2027 (estimated)
Last update
Jul 30, 2026

Study contacts

Holly Crandall, BSN
Contact
hrking1@iu.edu
13172786200

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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