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In the ITT analysis of 1,070 patients, the response rate (NASH resolution without fibrosis worsening) was 19.2% for patients who received elafibranor at 120 mg compared to 14.7% for the placebo arm

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Qualification elements included the semaglutide concentrationtime profiles, covariates, dosing conditions, consistency between oral and s.c./i.v

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