A Study Evaluating GS-9620 in Treatment Naive Subjects With Chronic Hepatitis C

PHASE1CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

December 31, 2012

Study Completion Date

December 31, 2012

Conditions
Hepatitis C
Interventions
DRUG

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.

DRUG

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).

Trial Locations (11)

10019

CliniLabs, New York

19139

CRI Worldwide, LLC, Philadelphia

32720

Avail Clinical Research, LLC, DeLand

32809

Orlando Clinical Research Center, Orlando

64131

Kansas City Gastroenterology and Hepatology, Kansas City

72211

Woodland International Research Group, Little Rock

78215

Alamo Medical Research, San Antonio

84106

Lifetree Clinical Research, Salt Lake City

08009

Comprehensive Clinical Research, Berlin

08046

CRI Worldwide, LLC, Willingboro

00909

Fundacion De Investigacion De Diego, Santurce

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY