drugset / Trial / NCT00684008

Safety Study of IL-7 in Recipients of a Hemopoietic Stem Cell Transplant Peripheral Blood Stem Cell Transplant

NCT00684008

Phase 1 Completed 12 enrolled Cytheris SA
NaSingle-groupOpen-labelTreatment

Summary

This is a phase I inter-patient dose escalation open labeled study assessing multiple doses of CYT107 in patients of at least 15 years of age, who are recipients of HLA matched ex vivo T cell depleted bone marrow or peripheral blood stem transplants. The dose escalation design is aimed at establishing the absence of significant toxicity and to define a biologically active dose in this patient population. At each dose level, eligible patients will receive 3 doses of CYT107 injected subcutaneously (under the skin of the arm, legs, or stomach) once a week for 3 weeks. Groups of three patients will be entered at each dose level of CYT107. Three dose levels are planned: 10 mcg/kg/week, 20 mcg/kg/week and 30 mcg/kg/week. Three patients must complete day 42 of the study at a dose level without a dose limiting toxicity (DLT) before there is escalation to the next dose level.

Timeline

Start
2008-03
Primary completion
Completion
2011-04

Drugs

EvaluationDrugModalityDoseRoute
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