Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination (FDC) With and Without Ribavirin for the Treatment of HCV



Status:Completed
Conditions:Hepatitis
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - Any
Updated:11/18/2018
Start Date:September 2012
End Date:April 2014

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A Phase 3, Multicenter, Randomized, Open-Label Study to Investigate the Efficacy and Safety of Sofosbuvir/GS-5885 Fixed-Dose Combination (FDC) +/- Ribavirin for 12 and 24 Weeks in Treatment-Naive Subjects With Chronic Genotype 1 HCV Infection.

The purpose of this study is to evaluate the safety, tolerability, and antiviral efficacy of
ledipasvir (LDV)/sofosbuvir (SOF) fixed-dose combination (FDC) tablets with or without
ribavirin (RBV) administered for 12 and 24 weeks in treatment-naive subjects with chronic
genotype 1 HCV infection.


Inclusion Criteria:

- Age ≥ 18, with chronic genotype 1 HCV infection

- HCV treatment-naive

- HCV RNA > 10,000 IU/mL at screening

- Cirrhosis determination; a liver biopsy may be required

- Screening laboratory values within defined thresholds

- Use of two effective contraception methods if female of childbearing potential or
sexually active male

Exclusion Criteria:

- Pregnant or nursing female or male with pregnant female partner

- Co-infection with HIV or hepatitis B virus (HBV)

- Current or prior history of clinical hepatic decompensation

- Hepatocellular carcinoma (HCC) 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 subject treatment, assessment or compliance with the protocol
We found this trial at
54
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Atlanta, GA
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Fayetteville, North Carolina 28304
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Statesville, North Carolina 28677
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