drugset / Trial / NCT00624325

Subcutaneous Continuous Infusion of Interferon Alfa-2b and Ribavirin in Hepatitis C Genotype 1 Nonresponders

NCT00624325

Phase 2/3 Completed 30 enrolled Foundation for Liver Research
RandomizedParallel-groupOpen-labelTreatment

Summary

For chronic hepatitis C patients unresponsive to previous (PEG-)IFN/RBV combination therapy we propose continuous subcutaneous administration of high-dose IFN-a2b (Intron A®) for 48 weeks in combination with 15 mg/kg/day RBV (Rebetol®) and optimal management of side effects in order to maintain the highest possible dosages of both IFN-a2b and RBV for 48 weeks. We expect improved tolerability with continuous subcutaneous pump delivery of IFN-a2b compared to thrice weekly or daily subcutaneous injection of IFN-a2b, and increased antiviral activity and biologic potency due to sustained and higher levels of a fully potent interferon protein.

Timeline

Start
2007-07
Primary completion
2010-06
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject interferon alfa-2b Protein / enzyme biologic 6e+06 iu Subcutaneous
Subject interferon alfa-2b Protein / enzyme biologic 9e+06 iu Subcutaneous
Subject interferon alfa-2b Protein / enzyme biologic 1.2e+07 iu Subcutaneous