drugset / Trial / NCT00322842

Treatment With AMD3100 (Plerixafor) in Non-Hodgkin's Lymphoma and Multiple Myeloma Patients

NCT00322842

Phase 2 Completed 35 enrolled Genzyme, a Sanofi Company AnorMED · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study evaluates the safety of plerixafor and other outcomes that are purely exploratory in nature. One other pre-specified outcome is to evaluate an interval of 10-11 hours between dosing with plerixafor and the beginning of apheresis to determine if there will be at least a 2-fold increase in circulating CD34+ cells. Data from this protocol will assist in the determination of the dosing schedule for future studies.

Timeline

Start
2004-09
Primary completion
2007-02
Completion
2007-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Plerixafor Small molecule 240 ug/kg Subcutaneous
Background Granulocyte colony-stimulating factor Protein / enzyme biologic 10 ug/kg Subcutaneous