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On March 14, 2024, resmetirom (Rezdiffra) became the first drug approved by the U.S. FDA for treating patients with noncirrhotic nonalcoholic steatohepatitis (NASH; recently renamed metabolic dysfunction–associated steatohepatitis, or MASH) and moderate-to-advanced hepatic fibrosis.1 This drug is an agonist of thyroid hormone receptor-β; agonists of this receptor in the liver promote hepatic fat metabolism and prevent hepatic injury resulting from lipotoxicity.
The pivotal manufacturer-sponsored randomized trial that led to FDA approval (MAESTRO-NASH) was reviewed recently in NEJM Journal Watch.2 In brief, nearly 1000 patients with biopsy-proven NASH (fibrosis stages 2 or 3) received resmetirom or placebo, taken orally once daily; participan…