This blog is all about current FDA approved drugs to treat the hepatitis C virus (HCV) with a focus on treating HCV according to genotype, using information extracted from peer-reviewed journals, liver meetings/conferences, and interactive learning activities.
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Friday, April 29, 2011
Merck Executive Sees FDA OK, Launch Of Boceprevir Hepatitis C Drug In May
By Peter Loftus
Of DOW JONES NEWSWIRES
Merck & Co. (MRK) expects to launch a new hepatitis C drug in May, pending U.S. regulatory approval, an executive said Friday.
"We are ready to launch," Adam Schechter, president of Merck;s global human health unit, told analysts on a conference call. "We believe we have completed the studies required for approval, and we anticipate to launch in May."
On Wednesday, a Food and Drug Administration advisory panel unanimously recommended the agency approve Merck's drug, boceprevir, which Merck proposes to sell under the brand Victrelis. An FDA decision is expected by mid-May.
An FDA committee also recommended approval of a competing hepatitis C drug, telaprevir, from Vertex Pharmaceuticals Inc. (VRTX) and Johnson & Johnson (JNJ).
Analysts see a multi-billion-dollar market for this new crop of hepatitis C drugs, with the Vertex/J&J drug having a competitive edge due to superior clinical-trial data.
-Peter Loftus, Dow Jones Newswires; +1-215-982-5581; peter.loftus@dowjones.com
(END) Dow Jones Newswires
April 29, 2011 09:18 ET (13:18 GMT)
Copyright (c) 2011 Dow Jones & Company, Inc.
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