drugset / Trial / NCT01025596

Dose Escalation Study of IL-7 and Bi-therapy in HCV Patients Resistant After 12 Weeks of Bi-therapy (ECLIPSE 1)

NCT01025596

Phase 1/2 Completed 10 enrolled Cytheris SA
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety of a new experimental drug, IL-7, in people with HCV infection resistant after 12 weeks of bi-therapy.

Timeline

Start
2007-05
Primary completion
2011-02
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Interleukin-7 Protein / enzyme biologic 3 ug/kg Subcutaneous
Subject Interleukin-7 Protein / enzyme biologic 10 ug/kg Subcutaneous
Subject Interleukin-7 Protein / enzyme biologic 20 ug/kg Subcutaneous
Subject Interleukin-7 Protein / enzyme biologic 30 ug/kg Subcutaneous