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