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Completed Phase 2 Interventional Results available

Antifibrotic Activity Of GI262570 In Chronic Hepatitis C Subjects

ClinicalTrials.gov ID: NCT00244751

Public ClinicalTrials.gov record NCT00244751. 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 Nov 6, 2026, 6:26 AM EST

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Official title

A Double-Blind, Randomized, Placebo-Controlled Multi-Center, Phase II Parallel Dose-Ranging Study to Assess the Antifibrotic Activity of GI262570 in Chronic Hepatitis C Subjects With Hepatic Fibrosis Who Have Failed Prior Antiviral Therapy

Brief summary

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

The purpose of this study is to examine the safety and effectiveness of GI262570 compared to placebo (a pill that looks exactly like GI262570 but contains no active medicine) in improving specific tests that indicate the degree of liver fibrosis (scarring). Subjects who are enrolled in the study must have had prior treatment with interferon (either pegylated or standard interferon) plus ribavirin for at least 12 weeks to treat their hepatitis C, but either failed to clear the virus or didn't tolerate the treatment.

Study identification

NCT ID
NCT00244751
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
265 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
40 Years to 70 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
Nov 2, 2005 (Actual)
Primary completion
Mar 13, 2008 (Actual)
Completion
Mar 13, 2008 (Actual)
Last update posted
Dec 11, 2017

2005 – 2008

United States locations

U.S. sites
58
U.S. states
23
U.S. cities
48
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294-0005 —
GSK Investigational Site Tucson Arizona 85719 —
GSK Investigational Site North Little Rock Arkansas 72117 —
GSK Investigational Site Bakersfield California 93301 —
GSK Investigational Site La Jolla California 92024 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Newport Beach California 92663 —
GSK Investigational Site Pasadena California 91105 —
GSK Investigational Site Sacramento California 95825 —
GSK Investigational Site San Clemente California 92673 —
GSK Investigational Site San Francisco California 94121 —
GSK Investigational Site Santa Clara California 95051 —
GSK Investigational Site Englewood Colorado 80113 —
GSK Investigational Site Washington D.C. District of Columbia 20010 —
GSK Investigational Site Fort Lauderdale Florida 33308 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Orlando Florida 32804 —
GSK Investigational Site Sarasota Florida 34243 —
GSK Investigational Site Atlanta Georgia 30033 —
GSK Investigational Site Atlanta Georgia 30308 —
GSK Investigational Site Atlanta Georgia 30309 —
GSK Investigational Site Marietta Georgia 30060 —
GSK Investigational Site Honolulu Hawaii 96817 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Lutherville-Timonium Maryland 21093 —
GSK Investigational Site Boston Massachusetts 02111 —
GSK Investigational Site Boston Massachusetts 02114 —
GSK Investigational Site Boston Massachusetts 02215 —
GSK Investigational Site Worcester Massachusetts 01655 —
GSK Investigational Site Ann Arbor Michigan 48109 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site St Louis Missouri 63104 —
GSK Investigational Site Binghamton New York 13901 —
GSK Investigational Site Manhasset New York 11030 —
GSK Investigational Site New York New York 10003 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site New York New York 10032 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site The Bronx New York 10468 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Durham North Carolina 27710 —
GSK Investigational Site Cincinnati Ohio 45219 —
GSK Investigational Site Cincinnati Ohio 45267-0595 —
GSK Investigational Site Cleveland Ohio 44195 —
GSK Investigational Site Tulsa Oklahoma 74104 —
GSK Investigational Site Hershey Pennsylvania 17033-0850 —
GSK Investigational Site Lancaster Pennsylvania 17604-3200 —
GSK Investigational Site Dallas Texas 75390-8887 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site San Antonio Texas 78215 —
GSK Investigational Site Charlottesville Virginia 22908 —
GSK Investigational Site Fairfax Virginia 22031 —
GSK Investigational Site Richmond Virginia 23249 —
GSK Investigational Site Richmond Virginia 23298 —

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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00244751, 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 Dec 11, 2017 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00244751 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →