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Clinical Trial Summary

enrolled participants were treated orally with SOF plus a fixed dose combination of OBV/PTV/r plus RBV.


Clinical Trial Description

Enrolled participants were treated orally with SOF plus a fixed dose combination of Sofosbuvir/Ombitasvir/Paritaprevir/ Ritonavir plus Ribavirin (OBV/PTV/r plus RBV), which was administered orally based on the participants' tolerability. The primary end point was a sustained virological response (HCV RNA level < 15 IU/ mL), observed 12 weeks after the end of the treatment (SVR12). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04391985
Study type Interventional
Source Beni-Suef University
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 1, 2017
Completion date October 31, 2017

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