Efficacy and Safety of Ledipasvir/Sofosbuvir Fixed-Dose Combination for 12 Weeks in Subjects With Chronic Genotype 1 or 4 HCV and HIV-1 Co-infection
Status: | Completed |
---|---|
Conditions: | HIV / AIDS, HIV / AIDS, Hepatitis, Hepatitis |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/18/2018 |
Start Date: | February 2014 |
End Date: | December 2015 |
A Phase 3, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Sofosbuvir/Ledipasvir Fixed-Dose Combination for 12 Weeks in Subjects With Chronic Genotype 1 or 4 Hepatitis C Virus (HCV) and Human Immunodeficiency Virus (HIV)-1 Co-infection
This study will evaluate the antiviral efficacy, safety, and tolerability of
ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) administered for 12 weeks in
hepatitis C virus (HCV) treatment-naive and treatment-experienced (including treatment
intolerant) participants with chronic genotype 1 or 4 HCV infection who are co-infected with
HIV-1.
Participants who experience confirmed post-treatment virologic failure (relapse) at or before
Posttreatment Week 24 may be eligible to be enrolled in the Retreatment Substudy to receive
LDV/SOF plus ribavirin (RBV) for 24 weeks.
ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) administered for 12 weeks in
hepatitis C virus (HCV) treatment-naive and treatment-experienced (including treatment
intolerant) participants with chronic genotype 1 or 4 HCV infection who are co-infected with
HIV-1.
Participants who experience confirmed post-treatment virologic failure (relapse) at or before
Posttreatment Week 24 may be eligible to be enrolled in the Retreatment Substudy to receive
LDV/SOF plus ribavirin (RBV) for 24 weeks.
Inclusion Criteria:
- HCV RNA ≥ 10,000 IU/mL at screening
- HCV genotype 1 or 4
- HIV-1 infection
- Cirrhosis determination, a fibroscan or liver biopsy may be required
- Screening laboratory values within defined thresholds
- Use of protocol specified method(s) of contraception if female of childbearing
potential or sexually active male
Exclusion Criteria:
- Clinically-significant illness (other than HCV or HIV) or any other major medical
disorder that may interfere with subject treatment, assessment, or compliance with the
protocol
- Current or prior history of clinical hepatic decompensation, hepatocellular carcinoma
(HCC), or other malignancy (with the exception of certain resolved skin cancers)
- Hepatitis B virus (HBV) infection
- Pregnant or nursing female
- Chronic use of systemically administered immunosuppressive agents
We found this trial at
35
sites
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