51
Participants
Start Date
March 31, 2012
Primary Completion Date
December 31, 2012
Study Completion Date
December 31, 2012
Single Ascending Dose Cohorts GS-9620
This study will enroll cohorts of 6 eligible, unique subjects per cohort, randomized to either active drug or placebo (5:1) within each cohort. Dose cohorts may be dosed with one of up to 4 possible total weekly doses (0.3 mg, 1 mg, 2 mg, 4 mg). Subjects in Single Ascending Dose (SAD) Cohorts will receive a single dose of GS-9620.
Multiple Ascending Dose Cohorts GS-9620
This study will enroll cohorts of 6 eligible, unique subjects per cohort, randomized to either active drug or placebo (5:1) within each cohort. Subjects in Multiple Ascending Dose (MAD) Cohorts will receive GS-9620 once weekly for two weeks (QW x 2 doses).
CliniLabs, New York
CRI Worldwide, LLC, Philadelphia
Avail Clinical Research, LLC, DeLand
Orlando Clinical Research Center, Orlando
Kansas City Gastroenterology and Hepatology, Kansas City
Woodland International Research Group, Little Rock
Alamo Medical Research, San Antonio
Lifetree Clinical Research, Salt Lake City
Comprehensive Clinical Research, Berlin
CRI Worldwide, LLC, Willingboro
Fundacion De Investigacion De Diego, Santurce
Lead Sponsor
Gilead Sciences
INDUSTRY