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Vertex is developing its own candidate - VX-135 - to competewith next-generation hepatitis C regimens. But it suffered asetback last week when the U.S. Food and Drug Administration puta hold on the U.S. trial of the 200-milligram dose of the drug.The FDA took the action following reports of potential livertoxicity in three patients who received the 400-mg dose ofVX-135 in a European study.
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