Efficacy and Safety of Ledipasvir/Sofosbuvir, With or Without Ribavirin, in HCV Infected Participants Who Have Failed Prior Treatment With Sofosbuvir-based Therapies
Status: | Terminated |
---|---|
Conditions: | Infectious Disease, Hepatitis |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/18/2018 |
Start Date: | November 11, 2015 |
End Date: | May 29, 2017 |
A Phase 3b, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Ledipasvir/Sofosbuvir, With or Without Ribavirin, in HCV Infected Subjects Who Have Failed Prior Treatment With Sofosbuvir-based Therapies
The primary objective of this study is to evaluate the efficacy, safety, and tolerability of
ledipasvir/sofosbuvir (LDV/SOF) fixed dose combination (FDC) for 12 weeks with or without
ribavirin (RBV) in participants without cirrhosis, and LDV/SOF FDC for 12 weeks with RBV or
LDV/SOF FDC for 24 weeks without RBV in participants with cirrhosis.
ledipasvir/sofosbuvir (LDV/SOF) fixed dose combination (FDC) for 12 weeks with or without
ribavirin (RBV) in participants without cirrhosis, and LDV/SOF FDC for 12 weeks with RBV or
LDV/SOF FDC for 24 weeks without RBV in participants with cirrhosis.
Key Inclusion Criteria:
- HCV RNA > 15 IU/mL at screening
- HCV genotype 1 or 4
- Chronic HCV infection (≥ 6 months)
- Prior virologic failure after treatment with SOF in combination with simeprevir (SMV)
± RBV or with RBV ± pegylated interferon (PEG)
- Cirrhotic and non-cirrhotic as determined by standard methods
- Male and female individuals of childbearing potential who engage in heterosexual
intercourse must agree to use protocol specified method(s) of contraception
Key Exclusion Criteria:
- Prior exposure to approved or experimental non-structural protein (NS5A) inhibitors
- Prior exposure to nucleos(t)ide polymerase inhibitors, other than SOF
- Pregnant or nursing female or male with pregnant female partner
- Coinfection with HIV or hepatitis B virus
- Current or prior history of clinical hepatic decompensation
- Hepatocellular carcinoma or other malignancy (with exception of certain resolved skin
cancers)
- Chronic use of systemic immunosuppressive agents
- History of clinically significant illness or any other medical disorder that may
interfere with individual's treatment, assessment or compliance with the protocol
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
We found this trial at
36
sites
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