Trial Information
Summary: Randomized, Multicenter, Open Label, Phase IV Study Evaluating the Efficacy and Safety of 16-Week Versus 24-Week Treatment with PEGASYS in Combination with Copegus in Interferon-naïve Patients with Chronic Hepatitis C Genotype 2 or 3 Virus Infection
Stanford University is looking for volunteers 18 years or older
with chronic hepatitis C (genotype 2 or 3) who have never received
prior antiviral treatment for hepatitis C infection (e.g.,
interferon, ribavirin). This study will compare dosing regimens of
drug Pegasys in combination with Copegus.
The study provides free study-related physical exams,
medications and diagnostic tests. Pegasys is administered by
self-injection. Ability to come to Stanford area for multiple,
regular visits is also required. Subjects must meet study criteria
in order to participate.
Volunteers with chronic hepatitis C who are interested in
participation in this study directed by Emmet Keeffe, MD, Professor
of Medicine, Stanford University, should contact the liver research
office @ (650) 724-7057.
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Contact:
Dana Supan, RN, Research Nurse
Stanford University School of Medicine
703 Welch Road F-5
Palo Alto, CA 94304
Telephone: 650-724-7057
Fax: 650-498-5864
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Trial listings updated: June 1, 2008 at 5:43:56 AM