Genfit SA says its decision to push back the unblinding of its Phase III RESOLVE-IT study of elafibranor in non-alcoholic steatohepatitis (NASH) until it receives “insights” from the US Food and Drug Administration about statistical methodology is aimed at putting together the best possible new drug application (NDA).
Investors seem to have taken the news in stride; the company’s stock closed at $17.90 on 20 February and fell...
Welcome to Scrip
Create an account to read this article
Already a subscriber?