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
| Type | Name | Description |
|---|---|---|
| DRUG | sofosbuvir and daclatasvir | Sofosbuvir (SOF) 400 mg tablet administered orally once daily. Daclatasvir (DCV) 60 mg tablet administered orally once daily. |
| DRUG | ledipasvir/sofosbuvir | Ledipasvir/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.