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Terminated Phase 2 Interventional

Efficacy and Safety Study of GS-9450 Treatment for 6 Months in Patients With Chronic Hepatitis C Virus Infection

ClinicalTrials.gov ID: NCT00874796

Public ClinicalTrials.gov record NCT00874796. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 11:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of GS 9450 in Adults With Chronic Hepatitis C Virus Infection (GS-US-227-0106)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 2b, randomized, double-blind, parallel-group, placebo-controlled, multicenter study investigating the safety, tolerability and efficacy of two oral doses of GS-9450 in adults with chronic Hepatitis C Virus (HCV). Approximately 240 subjects 18-65 years of age who meet study entry criteria will be randomized (in other words, selected at random, like flipping a coin) to one of three treatment groups (80 subjects per treatment group) as follows:GS-9450 10 mg once daily,GS-9450 40 mg once daily, or matching placebo once daily. Following randomization, subjects will return within seven business days for a Baseline (Day 1) visit, at which time study medication will be dispensed and subjects will enter a 26 week treatment phase. During the treatment phase, subjects will receive study drug once daily for 24 weeks and then taper off of study drug over the following 2 weeks by receiving study drug once every other day for one week and then every 3 days for one week. Following completion of the treatment phase, subjects will enter a 4-week off-treatment follow-up phase.

Study identification

NCT ID
NCT00874796
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
307 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2009 (Type not available)
Primary completion
Apr 2010 (Actual)
Completion
Jul 2010 (Actual)
Last update posted
Feb 4, 2014

2009 – 2010

United States locations

U.S. sites
51
U.S. states
26
U.S. cities
51
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Tucson Arizona — —
Not listed Anaheim California — —
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Not listed Cypress California — —
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Not listed San Clemente California — —
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Not listed Washington D.C. District of Columbia — —
Not listed Hialeah Florida — —
Not listed Miami Florida — —
Not listed North Miami Beach Florida — —
Not listed Orlando Florida — —
Not listed Sarasota Florida — —
Not listed Tampa Florida — —
Not listed Decatur Georgia — —
Not listed Chicago Illinois — —
Not listed Indianapolis Indiana — —
Not listed Louisville Kentucky — —
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Not listed New Orleans Louisiana — —
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Not listed Baltimore Maryland — —
Not listed Boston Massachusetts — —
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Not listed Saint Louis Michigan — —
Not listed Plymouth Minnesota — —
Not listed Omaha Nebraska — —
Not listed Las Vegas Nevada — —
Not listed Hillsborough New Jersey — —
Not listed Morristown New Jersey — —
Not listed Santa Fe New Mexico — —
Not listed Johnson City New York — —
Not listed New York New York — —
Not listed Plainview New York — —
Not listed Cincinnati Ohio — —
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Not listed Philadelphia Pennsylvania — —
Not listed Providence Rhode Island — —
Not listed Chattanooga Tennessee — —
Not listed Germantown Tennessee — —
Not listed Dallas Texas — —
Not listed San Antonio Texas — —
Not listed Fairfax Virginia — —
Not listed Falls Church Virginia — —
Not listed Norfolk Virginia — —
Not listed Seattle Washington — —
Not listed Madison Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00874796, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 4, 2014 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00874796 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →