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Description
Published large human clinical-trial data is not available, so consumer time to results framings sit outside the public regulatory evidence base
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Nikolic 2009)
In a 72-week, double-blind phase 2 trial in patients with biopsy-confirmed NASH (legacy term) and fibrosis stage F1F3, once-daily subcutaneous semaglutide produced dose-dependent NASH resolution: 59% at the 0.4 mg dose versus 17% with placebo (a statistically significant difference)
