Celebrating 1 Year of Resmetirom, Progress in MASH/MASLD - Episode 4
In the fourth segment of this 6-part HCPLive RX Review, experts discuss the continued importance of diet and exercise for managing MASH.
On March 14, 2024, the US Food and Drug Administration (FDA) made history when it granted accelerated approval to Madrigal Pharmaceuticals’ resmetirom (Rezdiffra), making it the first and only treatment for noncirrhotic nonalcoholic steatohepatitis (NASH), now known as metabolic dysfunction-associated steatohepatitis (MASH).
One year later, resmetirom’s impact on clinical practice and patient care continues to evolve. In recognition of the anniversary of the landmark decision, the latest HCPLive RX Review spotlights a conversation between a trio of subject matter experts reflecting on the past year of having resmetirom as a treatment option for patients, remaining unmet needs in MASH management, and the evolving therapeutic pipeline poised to further transform care.
Estimated to affect more than 30% of the global population, MASLD is the most common chronic liver disease around the world. MASH represents an advanced stage of MASLD and has historically lacked treatment options beyond lifestyle changes with diet and exercise. In the absence of pharmacologic therapies, weight loss served as the cornerstone of disease management.
This changed in March 2024, when resmetirom became the first and only FDA-approved MASH therapeutic, earning accelerated approval for the treatment of noncirrhotic MASH with moderate to advanced fibrosis. Although lifestyle interventions continue to play a pivotal role in MASH care, as the thyroid hormone receptor-beta selective agonist is indicated in conjunction with diet and exercise, they are no longer the only tools available for disease management.
In the fifth segment of our 6-part HCPLive RX Review on the 1-year anniversary of resmetirom’s FDA approval and the evolving landscape of MASH management, moderator Jeff McIntyre raises the topic of noninvasive diagnostics and biomarkers, emphasizing their potential role beyond screening and diagnosis—particularly for patient monitoring. He goes on to ask panelists Mazen Noureddin, MD, MHSc, and Juan Pablo Arab, MD, about how advances in noninvasive tools are shaping patient selection, disease monitoring, and future treatment strategies.
Arab stresses that noninvasive methods are the future. While liver biopsy remains valuable, imaging techniques like transient elastography and MRI-PDFF, along with serum tests such as ELF, offer promising alternatives. He highlights the use of simple tools like FIB-4 combined with transient elastography to efficiently stratify risk in the large population affected by steatotic liver disease.
Noureddin agrees that current noninvasive tools are effective but notes the need for further refinement. Efforts are underway to streamline diagnosis, including machine learning models and advanced biomarkers to replace the current guideline-recommended two-step approach with FIB-4 and transient elastography or ELF.
He highlights research showing that noninvasive scores predict liver-related outcomes and correlate with clinical improvements—key for regulatory approval. A major next step is eliminating biopsy in clinical trials, with ongoing work to provide regulators with the necessary evidence.
Moderator:
Jeff McIntyre is the vice president of Liver Health Programs at the Global Liver Institute.
Panelists:
Mazen Noureddin, MD, MHSc, is a professor of medicine and a transplant hepatologist at Houston Methodist and director of the Houston Research Institute.
Juan Pablo Arab, MD, is an associate professor of medicine in the division of gastroenterology, hepatology, and nutrition at Virginia Commonwealth University School of Medicine
Noureddin has relevant disclosures with Altimmune, Madrigal Pharmaceuticals, Merck, Takeda, Terns, and others. Arab and McIntyre have no relevant disclosures.