drugset / Trial / NCT00266318

Study of High Dosage CIFN Plus RBV for HCV Genotype 1 Infected Patients Who Are Nonresponders to Prior Therapy

NCT00266318

Phase 4 Completed 40 enrolled Beth Israel Medical Center InterMune · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The main purpose of this study is to evaluate the safety and tolerability of combination therapy of daily interferon alfacon-1 (Infergen, CIFN) at high dosage (24 mcg) with ribavirin (based on body weight) for 48 weeks in HCV genotype 1 infected subjects, who are non-responders to previous pegylated interferon alfa plus ribavirin therapy. This is an open-label, multicenter study. All subjects will receive Infergen 24 mcg administered by injection daily plus ribavirin 800-1400 mg (based on body weight) administered by mouth daily for 48 weeks \* If any 5 of the first 10 subjects can not tolerate the 24 mcg daily dosage of Infergen by week 4, as determined by the principal investigator, then the dosage of Infergen will be changed to 15 mcg administered by injection daily plus ribavirin 800-1400 mg (based on body weight) administered by mouth daily for 48 weeks

Timeline

Start
2005-12
Primary completion
2007-05
Completion
2007-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Interferon Alfacon-1 Protein / enzyme biologic 15 ug Other
Subject Interferon Alfacon-1 Protein / enzyme biologic 24 ug Other
Subject Ribavirin Small molecule 800 mg Oral
Subject Ribavirin Small molecule 1400 mg Oral