Sofosbuvir With Ribavirin or Simeprevir With HCV GT4 Egyptian Patients

Status Completed

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

Clinical Trial Details

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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