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Clinical Trial Summary

The purpose of this study in HCV genotype 4-infected subjects with compensated cirrhosis is to assess the safety and to compare the percentage of subjects achieving a 12-week sustained virologic response (SVR12), [HCV ribonucleic acid (RNA) < lower limit of quantification (LLOQ) 12 weeks following treatment], to a clinically relevant threshold [based on SVR rates for HCV genotype 4-infected subjects treated with pegylated interferon (pegIFN)/RBV].

The 12 and 16-week arms have been fully enrolled. As of 19 May 2015, they were closed and the two 24-week arms were opened for enrollment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02265237
Study type Interventional
Source AbbVie
Contact
Status Completed
Phase Phase 3
Start date October 28, 2014
Completion date April 7, 2017

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