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Completed Phase 3 Interventional

Thymosin Plus PEG-Interferon in Hepatitis C Patients With Cirrhosis Who Did Not Respond to Interferon or Interferon Plus Ribavirin

ClinicalTrials.gov ID: NCT00039962

Public ClinicalTrials.gov record NCT00039962. 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 Sep 3, 2026, 9:49 AM EDT

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

Brief summary

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

Chronic hepatitis C infection is one of the leading causes of chronic liver disease in the United States. Approximately one-third of patients with hepatitis C infection develop cirrhosis of the liver, which can lead to liver failure or liver cancer. The current treatment for hepatitis C infection in previously untreated patients is successful in only about half of patients. There is no established therapy for non-responders. This is a randomized, double-blinded, multicenter trial to determine the effectiveness of thymosin alpha 1 (thymalfasin) 1.6 mg twice weekly plus PEGinterferon alfa-2a 180 ug/wk compared to placebo plus PEGinterferon alfa-2a in adults with chronic hepatitis C with early cirrhosis or progression to cirrhosis who are non-responders to previous treatment with interferon or interferon plus ribavirin. The definition of non-response requires a positive HCV RNA test at the end of a course of at least 12 weeks of therapy. Patients will receive treatment for 12 months, and will be followed-up for a further 6 months after the end of therapy

Study identification

NCT ID
NCT00039962
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
SciClone Pharmaceuticals
Industry
Enrollment
500 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Apr 30, 2002
Primary completion
Not listed
Completion
Not listed
Last update posted
Jan 14, 2008

Started 2002

United States locations

U.S. sites
54
U.S. states
27
U.S. cities
46
Facility City State ZIP Site status
University of Alabama - Knollwood Physician's Group Mobile Alabama
Mayo Clinic Scottsdale Arizona
Advanced Clinical Research Institute Anaheim California
Gastroenterology Associates of East Bay Medical Group Berkeley California
Scripps Clinic La Jolla California
Loma Linda University Medical Center Loma Linda California
Huntington Memorial Hospital Pasadena California
Kaiser Permanente Sacramento California
University of California, Davis Medical Center Sacramento California
California Pacific Medical Center San Francisco California
San Mateo Medical Center San Mateo California
Kaiser Permanente Santa Clara California
Arapahoe Gastroenterology Littleton Colorado
Walter Reed Army Medical Center Washington D.C. District of Columbia
Washington Hospital Center Washington D.C. District of Columbia
University of Florida Gainesville Florida
Mayo Clinic Jacksonville Florida
University Of Miami Center for Liver Diseases Miami Florida
Digestive Healthcare of Georgia Atlanta Georgia
Center for Digestive and Liver Health Savannah Georgia
Idaho Gastroenterology Associates Meridian Idaho
University of Chicago Hospital & Clinic Chicago Illinois
University of Louisville Louisville Kentucky
LSU Healthcare Network New Orleans Louisiana
Johns Hopkins University Baltimore Maryland
Chevy Chase Clinical Research Chevy Chase Maryland
Endoscopic Microsurgery Associates Towson Maryland
New England Medical Center Boston Massachusetts
William Beaumont Hospital Royal Oak Michigan
Mississippi Gastrointestinal Associates Jackson Mississippi
Bradley Freilich MD, LLC Kansas City Missouri
VAMC Kansas City Missouri
North Shore University Hospital Manhasset New York
NYU Gastroenterology & Hepatology New York New York
VA Harbor HealthCare System New York New York
Carolinas Center for Liver Disease Charlotte North Carolina
Duke University Medical Center Durham North Carolina
University of Cincinnati College of Medicine Cincinnati Ohio
Metro Health Medical Ctr. Cleveland Ohio
The Cleveland Clinic Foundation Cleveland Ohio
Oregon Health Sciences University Portland Oregon
Albert Einstein Medical Center Philadelphia Pennsylvania
Jefferson University Physicians Philadelphia Pennsylvania
University of Pennsylvania Philadelphia Pennsylvania
Advanced Clinical Research Providence Rhode Island
Medical University of South Carolina Charleston South Carolina
University of Tennessee Gastroenterology Memphis Tennessee
Austin Gastroenterology PA Austin Texas
Baylor University Medical Ctr. Dallas Texas
Baylor College of Medicine Houston Texas
Baylor, VAMC Houston Texas
Metropolitan Research Fairfax Virginia
McGuire DVAMC Richmond Virginia
Wisconsin Center for Advanced Research Milwaukee 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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00039962, 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 Jan 14, 2008 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00039962 live on ClinicalTrials.gov.

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