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Food and Drug Administration (FDA) granted accelerated approval to resmetirom for adults with non-cirrhotic MASH and stage F2F3 fibrosis, thereby establishing the first regulatory foothold in this therapeutic area [15]

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doi: 10.1080/19490976.2025.2517821 72 ZhangX.HuangL.FengW.XuD.ZengY

No participant in the trial simply took 2 mg for the entire study duration (unless they were in the placebo group, of course)

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