Anadys shares fell 35.5% to $3.80 in afternoon trading on April 21, after the US drug developer presented mixed early-stage data on ANA598, its investigational non-nucleoside polymerase inhibitor.
The agent demonstrated potent antiviral activity at all dose levels and was well tolerated in a Phase Ib study in which patients chronically infected with the hepatitis C virus were treated for three days. However, there were three cases of severe skin rash that led the affected patients to discontinue treatment.
Presented at the annual meeting of the European Association for the Study of the Liver in Copenhagen, Denmark, findings showed that ANA598 resulted in rapid and sustained reductions in HCV RNA with median reductions at end of treatment exceeding 2 log10 (>99%) at all dose levels. At 200mg twice-daily, the median viral load reduction was 2.4 log10 (range of 0.4 to 3.4); at 400mg bid, 2.3 log10 (range of 1.6 to 3.5); and at 800mg bid, 2.9 log10 (range of 2.2 to 3.4).
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