Treatment of chronic hepatitis C patients with the NS3/4A protease inhibitor danoprevir (ITMN-191/RG7227) leads to robust reductions in viral RNA: a phase 1b multiple ascending dose study.


Abstract

Danoprevir was safe and well tolerated when administered for 14 days in patients with chronic HCV genotype 1 infection.

Treatment resulted in sustained, multi-log(10) IU/ml reductions in HCV RNA in upper dose cohorts.

These results support further clinical evaluation of danoprevir in patients with chronic HCV.


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