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Resmetirom in Patients With MASH and HFpEF

StatusNot Yet Recruiting
PhasePhase 1
Started2026-09
View on ClinicalTrials.gov ↗
This Phase 1b multicenter randomized double-blind placebo-controlled study evaluates the safety, tolerability and hepatic pharmacodynamic effects of resmetirom in adults with metabolic dysfunction-associated steatohepatitis (MASH) and heart failure with preserved ejection fraction (HFpEF). Participants are randomized 2:1 to resmetirom or placebo for 24 weeks.
Trial Details
NCT Number NCT07830758
Lead Sponsor Madrigal Pharmaceuticals, Inc.
Conditions MASH - Metabolic Dysfunction-Associated Steatohepatitis, Heart Failure With Preserved Ejection Fraction (HFPEF)
Enrollment 90 participants
Start Date 2026-09
Primary Completion 2027-11 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2026-09-21