Genfit May Be Gaining An Edge In NASH Race

With Intercept encountering safety concerns for Ocaliva and mixed data for Gilead's and Allergan's NASH candidates, Genfit may hold an advantage with NASH clearance ability and clean safety profile.

Liver

Genfit SA may now hold the clearest path to market of the four companies in Phase III for non-alcoholic steatohepatitis (NASH), due largely to the misfortunes of its competitors. Those setbacks, and the progress being made in NASH, were discussed on the sidelines of the American Association for the Study of Liver Diseases annual meeting.

Presumed leader Intercept Pharmaceuticals Inc. has battled safety issues for its candidate Ocaliva (obeticholic acid) due to real-world treatment experience with the drug in primary biliary cholangitis (PBC), and Gilead Sciences Inc. and Allergan PLC recently have unveiled data for their candidates that could be called mixed at best. But Genfit chugs along with its strategy to advance elafibranor to an anticipated 1,000-patient interim look at its ongoing Phase III RESOLVE-IT study in 2019

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