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Diagnostic accuracy of screening tests for diabetic peripheral neuropathy: an umbrella review

Harrison and colleagues conducted a phase III trial in adults with NASH and fibrosis who received resmetirom once daily at a dose of 80 mg, 100 mg, or placebo for 52 weeks: 25.9% of the patients receiving 80 mg of resmetirom and 29.9% of the patients receiving 100 mg had MASH resolution compared to 9.7% in the placebo group

Laboratory assessment Specimen Collection: Blood collection was performed with care to avoid stasis, hemolysis or contamination by tissue fluids, or exposure to glass

(2025, May 12)

Kalluri, H., & Banga, A

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