drugset / Trial / NCT01288573

A Combined Study in Pediatric Cancer Patients for Dose Ranging and Efficacy/Safety of Plerixafor Plus Standard Regimens for Mobilization Versus Standard Regimens Alone

NCT01288573

Phase 1/2 Completed 46 enrolled Genzyme, a Sanofi Company Sanofi · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multi-site study with plerixafor in pediatric cancer patients. The study will be conducted in 2 stages: * Stage 1 is a dose-escalation study. * Stage 2 is an open-label, randomized, comparative study using the appropriate dosing regimen identified in the Stage 1 dose-escalation study. All participating patients will receive a standard mobilization regimen as per study site practice guidelines (either chemotherapy plus once daily granulocyte-colony stimulating factor (G-CSF) or once daily G-CSF alone). The only change to the standard mobilization regimen is the addition of plerixafor treatment prior to apheresis for all patients in Stage 1 (dose escalation), and for those patients randomized to the plerixafor plus standard mobilization treatment arm in Stage 2 (randomized, comparative). Stage 1 will enroll at least 27 patients. Stage 2 will enroll at least 40 patients.

Timeline

Start
2014-03-03
Primary completion
2017-05-09
Completion
2017-05-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Plerixafor Small molecule 160 ug/kg Subcutaneous
Subject Plerixafor Small molecule 240 ug/kg Subcutaneous
Subject Plerixafor Small molecule 320 ug/kg Subcutaneous