Sofosbuvir/Velpatasvir Fixed-Dose Combination in Adults With Chronic HCV Infection and Child-Pugh Class B Cirrhosis
Status: | Completed |
---|---|
Conditions: | Infectious Disease, Gastrointestinal, Hepatitis, Hepatitis |
Therapuetic Areas: | Gastroenterology, Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/17/2018 |
Start Date: | July 2014 |
End Date: | November 2015 |
A Phase 3, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed-Dose Combination in Subjects With Chronic HCV Infection and Child-Pugh Class B Cirrhosis
The primary objectives of this study are to evaluate the efficacy, safety, and tolerability
of sofosbuvir (SOF)/velpatasvir (VEL) fixed dose combination (FDC) with and without ribavirin
(RBV) for 12 weeks and SOF/VEL FDC for 24 weeks in adults with chronic hepatitis C virus
(HCV) infection and Child-Pugh-Turcotte (CPT) class B cirrhosis.
of sofosbuvir (SOF)/velpatasvir (VEL) fixed dose combination (FDC) with and without ribavirin
(RBV) for 12 weeks and SOF/VEL FDC for 24 weeks in adults with chronic hepatitis C virus
(HCV) infection and Child-Pugh-Turcotte (CPT) class B cirrhosis.
Inclusion Criteria:
- Willing and able to provide written informed consent
- HCV RNA > 10^4 IU/mL at screening
- Chronic HCV infection (≥ 6 months)
- Confirmed CPT class B (7-9) at screening
Exclusion Criteria:
- Current or prior history of solid organ transplantation, significant pulmonary
disease, significant cardiac disease, or porphyria
- Inability to exclude hepatocellular carcinoma (HCC) by imaging within 6 months of
baseline/Day 1
- Infection with hepatitis B virus (HBV) or human immunodeficiency virus (HIV)
- Screening ECG with clinically significant abnormalities
- Prior exposure to SOF or any other nucleotide analogue HCV nonstructural protein 5B
(NS5B) inhibitor or any HCV NS5A inhibitor
- Laboratory results outside of acceptable ranges at screening
We found this trial at
50
sites
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