Assessing the Efficacy and Safety of Rosiglitazone Added to Standard Therapy for Hepatitis C Genotype 1 With Fatty Liver

NCT ID: NCT00274495

Last Updated: 2007-11-01

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE4
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-01-31
• Study Completion Date: 2007-10-31

Brief Summary

To study the effectiveness and safety of adding Rosiglitazone, an insulin sensitizing agent to people with chronic hepatitis C infection genotype 1 with fatty liver disease, who are being treated with standard therapy. Standard therapy consists of weekly pegylated interferon injections and daily ribavirin pills, whose dosage is weight based. This regimen in genotype 1 patients is effective in only 45% of patients at best. In addition, this therapy must be given for 48 weeks to be effective and has alot of side-effects. One risk factor for a poor response is fatty liver. Rosiglitazone has been shown to be effective in the treatment of patients with fatty liver alone. This study hopes to show that the addition of Rosiglitazone to the standard therapy in genotype 1 patients with fatty liver disease will increase effectiveness of the standard therapy of hepatitis C.

Detailed Description

Eligible thirty subjects will be randomized in a double blinded fashion to either Rosiglitazone 4mg pills twice a day versus placebo for six weeks. Then after this six week period, both groups will be treated for 48 weeks of standard therapy for hepatitis C consisting of Pegasys 180mcq weekly injections with Ribavirin 1,000mg-1,200mg daily depending if the subject weights less than 75 kg will then receive the lower dosage. In addition, the subjects will be continued on Rosiglitazone or placebo for the 48 weeks.

The subjects will be monitored for side-effects by history taking and blood testing at predetermined time periods during the study. If the viral load has not dropped more than two log at week 12 of standard therapy for hepatitis C then therapy will be stopped and the subject is considered a treatment failure. Similarly, if there was a greater than two log drop in the viral load at week 12 but there is still virus present in the blood at week 24 then therapy is stopped and the subject is considered treatment failure. If the virus is undetectable in the blood at week 12 and 24 then therapy is continued for the full 48 weeks. If the virus is detectable at week 48 then the subject is considered a treatment failure.

After this 48 week treatment period and the virus is still undetectable, there is a follow-up period consisting of 24 weeks off therapy. At the end of the 24 weeks, blood will be tested for the virus and if the virus is not present then the subject has a sustained viral response and is a treatment success.

During therapy if the subject becomes significantly anemic Procrit 40,000Units weekly injections will be started. Similarly, if the white blood cell count drops below a certain level then weekly Neupogen 300mcq injections will be started. In addition, if there is mild depressive symptoms treatment will be started but if there is major depressive symptoms, then therapy will be stopped and a referral to a psychiatrist will be made.

Conditions

Chronic Hepatitis C Infection; Fatty Liver

Keywords

Genotype 1; Metabolic syndrome; Insulin resistance

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

Rosiglitazone and Pegasys/Ribavirin

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Men and women at least 21 years of age.
• Positive serum hepatitis C RNA for at least 6 months.
• Naive to any therapy for hepatitis C infection.
• Significant steatosis or fat on the liver biopsy.
• Genotype 1 patients.

Exclusion Criteria

• Subjects with decompensated liver disease.
• Hemoglobin <12g/dl.
• WBC<2,000mm3.
• ANC<1,000mm3.
• Platelet count<50,000/mm3.
• Creatinine>1.5mg/dl.
• Albumin<2.5g/dl.
• Bilirubin>4mg/dl.
• HIV or hepatitis B co-infection.
• History of other liver disease besides fatty liver disease.
• History of unstable cardiac or cerebrovascular disease.
• History of significant psychiatric disorders.
• Alcohol or drug abuse within last year.
• Pregnant or lactating women or men whose sexual partner is pregnant or lactating.
• Taking of insulin or oral hypoglycemic agents within six months of the study.
• Uncontrolled thyroid disorder.
• History of malignancy within the past 5 years unless cured by surgery.
• History of autoimmune disorder or organ transplantations requiring immunosuppression.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Beth Israel Medical Center

OTHER

Sponsor Role: lead

Principal Investigators

Douglas Meyer, M.D.

Role: PRINCIPAL_INVESTIGATOR

Beth Israel Medical Center

Henry C. Bodenheimer, M.D.

Role: STUDY_DIRECTOR

Beth Israel Medical Center

Locations

Beth Israel Medical Center - Philipps Ambulatory Care Center

New York, New York, United States

Countries

United States

Other Identifiers

098-04

Identifier Type: -

Identifier Source: org_study_id