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Therapeutic Areas: Gastroenterology | Immunology/Infectious Diseases
Disease Category: Hepatitis

Trial Information

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.

Dana Supan, RN, Research Nurse
Stanford University School of Medicine
703 Welch Road F-5
Palo Alto, CA 94304
Phone: 650-724-7057
Fax: 650-498-5864

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