Frank Duff, M.D., head of Roche's Clinical Development for Virology, said, "This trial represents an important step forward in the development of this oral direct-acting antiviral (DAA), and builds on the encouraging clinical safety and efficacy data generated to date."
Dan Welch, chairman, chief executive officer and president of InterMune, added, "We are very pleased to announce with our colleagues, Roche, the start of the global Phase IIb program of RG7227/ ITMN-191 in treatment-naive HCV patients. This study will significantly expand the clinical efficacy and safety database for this treatment, and in the first quarter of next year provide our first look at the rapid virologic response (RVR) rates associated with this triple therapy."
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