A Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Ranging Study Evaluating the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-6620 in Treatment Naïve Subjects with Chronic Hepatitis C Virus Infection.
Study Type
INTERVENTIONAL
Enrollment
90
Advanced Clinical Research Institute
Anaheim, California, United States
Axis Clinical Trials
Los Angeles, California, United States
Avail Clinical Research, LLC
DeLand, Florida, United States
Number of subjects with adverse events as a measure of safety and tolerability.
Number of subjects with HCV RNA viral response as a measure of antiviral activity.
Concentrations and pharmacokinetic parameters of GS-6620 and its metabolites will be measured.
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GS-6620 tablet, 100 mg QD, Fasted
GS-6620 tablet, 300 mg QD, Fasted
GS-6620 tablet, 900 mg QD, Fasted
GS-6620 tablet, 450 mg BID
GS-6620 tablet, 900mg , BID
GS-6620 tablet, 900 mg
University of Florida - Gainesville
Gainesville, Florida, United States
Orlando Immunology Center
Orlando, Florida, United States
Orlando Clinical Research Center
Orlando, Florida, United States
Saint Louis University
St Louis, Missouri, United States
CRI Worldwide
Philadelphia, Pennsylvania, United States
St. Luke Episcopal Hospital
Houston, Texas, United States
Alamo Medical Research
San Antonio, Texas, United States
...and 3 more locations