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Clinical Trial Summary

This open-label study will evaluate safety, pharmacokinetics and efficacy of a 12 or 24-week regimen of ombitasvir/paritaprevir/ritonavir and dasabuvir with or without ribavirin in HCV-genotype 1-infected subjects with an Estimated Glomerular Filtration Rate (eGFR) <30, including those on hemodialysis or peritoneal dialysis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02207088
Study type Interventional
Source AbbVie
Contact
Status Completed
Phase Phase 3
Start date September 23, 2014
Completion date December 6, 2016

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