None listed
Conditions
Interventions
Group C: Patients not responding or who relapsed to induction therapy of Interferon alfa 5 MU for 2 weeks followed by combination therapy (randomly selected).
C1: Interferon alfa-2b 10 MU subcutaneously daily for 4 weeks associated with ribavirin (induction period). From day 15, the dose of Interferon AIfa-2b will be reduced to 3 MU SC three times a week x 20 weeks and ribavirin will be continued at a dose of 1000 mg / day (patients 75 Kg). The dose of ribavirin is administered in two doses
Group B (Non-responders or patients who relapsed to combination therapy (randomly selected):
B1: Interferon alfa-2b 10 MU subcutaneously daily for 2 weeks associated with ribavirin (induction period). From day 15, the dose of Interferon Alfa-2b will be reduced to 3 MU SC three times a week x 22 weeks and ribavirin will be continued at a dose of 1000 mg / day (patients 75 Kg).
B2: Interferon alfa-2b 10 MU subcutaneously daily for 4 weeks associated with ribavirin (induction period). From d
Sponsors
SCHERING PLOUGH RESEARCH INSTITUTE,
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients with chronic hepatitis C. 2) Anti-HCV positive by enzyme immunoassay (ELIZA) of second generation or recombinant Immunoblot (RIBA).
Exclusion criteria
Exclusion criteria: Any other etiology of liver disease, based on clinical history and biopsy (if necessary), other than chronic hepatitis C.
Countries
Peru
Contacts
Public ContactOscar Barrenechea
SCHERING PLOUGH DEL PERU S.A.
Outcome results
None listed