Trial met primary endpoint with a statistically significant higher percentage of patients achieving a clinically meaningful cholestasis response compared to placebo
Elafibranor was well tolerated with a safety profile consistent with previous studies
Results position elafibranor as a potentially important new treatment option, where there is still high unmet need
Ipsen intends to submit regulatory applications for elafibranor following discussions with the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA)
GENFIT conference call (English and French) on June 30 at 8am ET / 1pm GMT / 2pm CET
GENFIT will host a conference call on June 30, 2023 at 8:00am ET / 1:00pm GMT / 2:00pm CET in English and in French
Both the English and French conference calls will be accessible on the investor page of our website, under the events section at https://ir.genfit.com/ or by calling 888-394-8218 (toll-free U.S. and Canada), 0800 279 0425 (toll-free UK) or 0805 101 219 (France) five minutes prior to the start time (confirmation code: 6752821). A replay will be available shortly after the call.
https://finance.yahoo.com/news/ipsen-genfit-announce-positive-results-050000395.html
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