drugset / Trial / NCT00624325
Subcutaneous Continuous Infusion of Interferon Alfa-2b and Ribavirin in Hepatitis C Genotype 1 Nonresponders
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |