Clinical Trials Directory

Trials / Completed

CompletedNCT02576314

Sofosbuvir Containing Regimens for the Treatment of Chronic HCV GT3 Infected Patients

Efficacy and Safety Study of Sofosbuvir Containing Regimens in Subjects With Chronic Hepatitis C Virus Genotype 3 Infection

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Humanity and Health Research Centre · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the safety, tolerability, and efficacy of Sofosbuvir containing regimens in treatment-naive or treatment-experienced patients with HCV genotype 3 infection.

Conditions

Interventions

TypeNameDescription
DRUGsofosbuvir and daclatasvirSofosbuvir (SOF) 400 mg tablet administered orally once daily. Daclatasvir (DCV) 60 mg tablet administered orally once daily.
DRUGledipasvir/sofosbuvirLedipasvir/sofosbuvir (LDV/SOF) 90 mg/400 mg fixed dose combination (FDC) tablet administered orally. once daily;

Timeline

Start date
2015-05-01
Primary completion
2017-12-31
Completion
2018-03-15
First posted
2015-10-15
Last updated
2018-03-19

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT02576314. Inclusion in this directory is not an endorsement.