CBEYOND
Brief description of study
Phase 3, Randomized, Controlled, Open-label Study to Compare the Efficacy and Safety of Bemnifosbuvir-Ruzasvir Fixed-dose Combination (BEM/RZR FDC) Versus Sofosbuvir-Velpatasvir Fixed-dose Combination (SOF/VEL FDC) in Subjects with Chronic Hepatitis C Virus (HCV) Infection
Detailed description of study
Penn researchers are looking for people who may be interested in taking part in the C-BEYOND clinical research study. The purpose of this study is to compare the safety and effectiveness of an investigational drug (study drug) with a comparator drug. The comparator drug is a generic version of a drug approved in the United States and Canada to treat HCV, but this generic version being used in the study has only been authorized in the United States. You may be eligible to participate in this HCV infection study if you:
• are 18–85 years of age,
• have a chronic HCV infection, and
• do not have a hepatitis B virus infection.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: 18 years - 85 years
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Gender: All
Documented HCV, No prior use of direct-acting antiviral (DAA) treatment
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