Trial Information

Summary: Severe Liver Fibrosis Due To Hepatitis C

A phase II, double blind, randomized, placebo-controlled, multicenter, study of the safety and anti-fibrotic efficacy of interon-gamma 1b (IFN-Y 1b) in patients with severe liver fibrosis or compensated cirrhosis due to hepatitis c.

You may be eligible to participate in the above clinical research study if you:

  • Have chronic hepatitis C
  • Are between the ages of 18 and 75 years of age
  • Have not benefited from prior treatment with interferon-alpha-based therapies or combinations of therapies
  • Are willing to undergo a liver biopsy
  • Have not been treated with interferon-alpha-based therapy within the past 12 months.
  • Do not have any of the following: autoimmune hepatitis, chronic hepatitis B, Wilson’s disease, drug-or toxin induced liver disease, alcohol-related liver disease, rheumatoid arthritis, systemic lupus, autoimmune thyroid disease, and are not HIV positive.

Contact:

Maly Tiev, Research Coordinator
Biomedical Research Alliance of New York
North Shore University Hospital
Manhasset, NY 11030
Telephone: 516-562-2061
Fax: 516-562-1688

Profile Page: Biomedical Research Alliance of New York, Manhasset, NY

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Trial listings updated: June 1, 2008 at 5:43:19 AM


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