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FDA approves Ocaliva for rare, chronic liver disease
FDA.gov On Friday, May 27, the U.S. Food and Drug Administration granted accelerated approval for Ocaliva (obeticholic acid) for the treatment of primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults with an inadequate ... Why Intercept Pharmaceuticals Inc (ICPT) is an Attractive Acquisition Target Intercept Pharmaceuticals (ICPT) Stock: FDA Approves Ocaliva 3 Reasons Goldman Sachs Still Neutral On Intercept Pharma |
from Health - Google News http://news.google.com/news/url?sa=t&fd=R&ct2=us&usg=AFQjCNE3aqFYCLuPAMxAvXjbBVmi1C2aog&clid=c3a7d30bb8a4878e06b80cf16b898331&cid=52779124035805&ei=8bJNV9DTE8qe3QGrtp64Bg&url=http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm503964.htm
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