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Clinical Trial Summary

This study will evaluate the safety and efficacy of ombitasvir/paritaprevir/ ritonavir and dasabuvir administered for 8 weeks in treatment-naïve participants with genotype 1b (GT1b) hepatitis C virus (HCV).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02582632
Study type Interventional
Source AbbVie
Contact
Status Completed
Phase Phase 3
Start date November 24, 2015
Completion date December 1, 2016

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