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Friday, May 25, 2012
Gilead Sciences Inc., of Foster City, Calif., said the European Medicines Agency validated its marketing authorization application (MAA) for cobicistat, submitted on April 26. Cobicistat is Gilead's pharmaco-enhancing agent to increase blood levels of certain commercially available protease inhibitors, including atazanavir (Reyataz, Bristol-Myers Squibb Co.) and darunavir (Prezista, Tibotec Pharmaceuticals), to enable once-daily dosing.
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