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Clinical Trial Summary

A total of 201 participants with chronic HCV GT4 infection were allocated into two groups. One group participants were treated with SOF plus RBV (24 weeks). The second group was treated with SOF plus SMV (12 weeks).


Clinical Trial Description

A total of 201 participants, treatment-naïve and experienced, with chronic HCV GT4 infection were allocated into two groups based on the type of the regimen used. All eligible participants were treated orally with SOF plus daily oral weight-based RBV (24 weeks; group 1), or SOF plus daily oral SMV (12 weeks; group 2). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04385407
Study type Interventional
Source Beni-Suef University
Contact
Status Completed
Phase Phase 2
Start date April 2015
Completion date July 2016

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