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Clinical Trial Summary

This study evaluates the efficacy and safety of ABT-450/r/ABT-267 with RBV in treatment-naive and treatment-experienced HCV GT4 subjects without or with compensated cirrhosis.


Clinical Trial Description

Non-cirrhotic subjects were directly enrolled into Arm A. Cirrhotic subjects were randomized to either Arm B (12 weeks of treatment) or Arm C (24 weeks of treatment). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02247401
Study type Interventional
Source AbbVie
Contact
Status Completed
Phase Phase 3
Start date November 4, 2014
Completion date August 1, 2016

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