USA-based Human Genome Sciences has reported that its Albuferon (albinterferon alfa-2b) met the primary endpoint in ACHIEVE 1, a Phase III trial in the treatment of hepatitis C.
Albuferon, in combination with ribavirin, was non-inferior to Swiss drug major Roche's Pegasys (peginterferon alfa-2a) in the randomized, multicenter, active-controlled trial in treatment-naive patients with genotype-1 chronic hepatitis C (p=0.0008).
48% (213/442) of subjects achieved sustained virological response in the Albuferon 900mcg group, versus 51% (225/441) in the Pegasys cohort. Patients receiving the active drug had comparable rates of serious and/or severe adverse events compared to the placebo arm (24% vs 23%).
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