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OpenTrials
Completed

NCT Number: NCT00084279

CIFN and IFN γ-1b With or Without Ribavirin for Treatment of Chronic Hepatitis C (Nonresponders)

To evaluate the safety and tolerability of two different doses of Consensus Interferon-Alpha and Interferon Gamma-1b with or without ribavirin in patients with chronic hepatitis C who are non-responders to PEG-IFN-a 2a or PEG-IFN-a 2b plus ribavirin.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed, written, informed consent from the patient or legal representative before any study-specific procedures are performed
  • Male or female 18 years of age or older
  • Chronic hepatitis C infection based on history of positive serum anti-HCV antibody and/or HCV RNA
  • Patients must have documented failure to respond to past treatment with PEG-Intron or Pegasys plus RBV.
  • Liver biopsy within 3 years of screening documenting chronic liver disease consistent with chronic hepatitis C

Exclusion criteria

  • Patients with any history of decompensated liver disease including but not restricted to portal hypertension as manifested by gastroesophageal varices, variceal bleeding, ascites, or encephalopathy
  • Specific laboratory abnormalities at Screening
  • Patients who were HCV RNA negative during prior pegylated interferon plus ribavirin treatment, but who relapsed during follow-up
  • Recent depression or psychiatric disorders
  • Known HIV infection or positive HIV antibody test at Screening
  • Chronic hepatitis B infection or positive hepatitis B surface antigen (HBsAg) at Screening
  • Unstable or uncontrolled thyroid disease
  • Presence or history of non-HCV chronic liver disease
  • History of unstable or deteriorating cardiovascular or cerebrovascular disease within 6 months prior to Screening
  • Current or history of neurologic disorder within a specified time frame
  • A disease known to cause significant alteration in immunologic function including hematological malignancy, sarcoidosis or autoimmune disorder (e.g. rheumatoid arthritis, systemic lupus erythematosis, leukemia, lymphoma, autoimmune thyroid disease, scleroderma, psoriasis, inflammatory bowel disease, multiple sclerosis etc.)
  • History of major organ transplantation (i.e., liver, kidney, lung, or heart) with an existing functional graft, including bone marrow transplant or stem cell transplant
  • Concurrent therapy with immunosuppressive drugs or cytotoxic agents such as cyclosporine, azathioprine, chronic systemic corticosteroids, or chemotherapeutic agent(s) (e.g., cyclophosphamide, methotrexate, or cancer chemotherapy) or radiation therapy
  • Pregnant or lactating women
  • Liver biopsy within the past three years documenting cirrhosis

Treatment and study plan

Consensus Interferon-Alpha, Interferon Gamma-1b, Ribavirin

Drug

interferon gamma-1b: 0.25 and 0.5 mL, SQ, 3x per week interferon alfacon: 0.3 mL and 0.5 mL, SQ, once a day Ribavirin: 2 capsules in a.m., 3 capsules in p.m.; daily

Primary outcomes

  1. Virologic response defined as >2 log (base 10) reduction in HCV RNA

    Time frame: 72 weeks

Sponsors and collaborators

Lead sponsor

InterMune

Industry

Registry information

Official study title

Safety and Tolerability of Consensus Interferon-Alpha (CIFN) Plus Interferon Gamma-1b (IFN-γ 1b) With or Without Ribavirin (RBV) in the Treatment of Patients With Chronic Hepatitis C Who Are Non-Responders to PEG-IFN-a (2a or 2b) Plus RBV

Important dates

Study start
2004
Study completion
2006
First posted
Jun 11, 2004
Registry last updated
Jul 3, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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