Brief: US FDA panel votes against accelerated approval of Intercept's fatty liver drug
May 19 (Reuters) - Intercept Pharmaceuticals Inc
ICPT.O :
* US FDA ADVISERS SAY BENEFITS OF INTERCEPT'S DRUG DO NOT
OUTWEIGH
RISKS IN NASH PATIENTS WITH FIBROSIS BASED ON CURRENT DATA
* US FDA ADVISERS VOTE TO DEFER APPROVAL OF INTERCEPT'S DRUG
FOR
NASH PATIENTS WITH LIVER FIBROSIS UNTIL MORE DATA IS AVAILABLE
Further company coverage: ICPT.O
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Intercept Pharmaceuticals
See all newsIntercept Pharmaceuticals Inc expected to post a loss of 44 cents a share - Earnings Preview
U.S. RESEARCH ROUNDUP-Digitalbridge Group, Huntington Ingalls Industries, Workday
U.S. RESEARCH ROUNDUP-Docusign, Immunovant, Liberty Energy
U.S. STOCKS ON THE MOVE-Amazon, United Parcel Service, Nike
U.S. STOCKS ON THE MOVE-BullFrog AI, Soleno,