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56 percent of individuals receiving ANA598 plus SOC achieved undetectable levels of virus at week 4.

Anadys Pharmaceuticals reviews positive 4-week results from its ANA598 Phase II study for HCV Anadys Pharmaceuticals, Inc. today announced preliminary results from a well planned interim analysis of data at four weeks for the first dose cohort, 200 mg bid, in an ongoing Phase II study of ANA598 in combination with pegylated interferon and ribavirin in HCV sufferers. 56 percent of individuals receiving ANA598 plus SOC achieved undetectable levels of virus at week 4, referred to as Rapid Virological Response or RVR, compared to 20 percent of patients receiving placebo plus SOC www.sildenafilcitrate.net .

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