Intercept: Company Statement on FDA Advisory Committee Meeting

MORRISTOWN, N.J., Sept. 13, 2024 (GLOBE NEWSWIRE) - The Gastrointestinal Drugs Advisory Committee (GIDAC) of the U.S. Food and Drug Administration (FDA) met today to discuss Intercept's supplemental New Drug Application (sNDA) for OCALIVA® (obeticholic acid, OCA) for the treatment of primary biliary cholangitis (PBC) - a rare, progressive disease that disproportionally affects women. The [...]