Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Oct 18, 2026, 7:38 PM 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
May 2002 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Jan 15, 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 15, 2008 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00039962 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →