A Phase 3, Global, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Safety and Efficacy of Sofosbuvir/Velpatasvir/GS-9857 Fixed-Dose Combination for 12 Weeks in Direct-Acting Antiviral-Experienced Subjects with Chronic HCV Infection (POLARIS 1: GS-US-367- 1171)
A study for patients with Chronic HCV Infection using study drugs Sofosbuvir, Velpatasvir and GS-9857
Sponsor: Gilead
Enrolling: Male and Female Patients
IRB Number: AAAQ4250
U.S. Govt. ID: NCT02607735
Contact: Theresa Lukose: 212-305-6758 / tt2103@cumc.columbia.edu
Additional Study Information: The purpose of this study is to evaluate the efficacy, safety, and tolerability of SOF/VEL/GS- 9857 FDC in patients infected with Hepatitis C (HCV), and previously treated unsuccessfully. Information about any side effects that may occur will also be collected.
This study is closed
Investigator
Elizabeth Verna, MD
Do You Qualify?
Have you been diagnosed with Chronic HCV Infection? Yes No
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For more information, please contact:
Theresa Lukose
tt2103@cumc.columbia.edu
212-305-6758
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