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Exploring the MAESTRO-NASH trial data Both primary endpoints were achieved in the two treatment arms of resmetirom (80 mg and 100 mg) at week 52

These mutants were resistant to FBXW7-mediated ubiquitination and degradation compared to ETV6-WT (Fig

The trial also showed a slower decline in eGFR and a lower risk of major cardiovascular events in the semaglutide group compared to placebo

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Patients can expect to leave the office unassisted the same day as the procedure