drugset / Trial / NCT00890500

Safety and Efficacy of ProHema Modulated Umbilical Cord Blood Units in Subjects With Hematologic Malignancies.

NCT00890500

Non-randomizedFactorialOpen-labelTreatment

Summary

The purpose of this research study is to determine the safety and efficacy of a reduced intensity conditioning regimen during a double umbilical cord blood unit transplant with one of the cord blood units modulated with ProHema.

Timeline

Start
2011-01
Primary completion
2013-05
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator ANTILYMPHOCYTE IMMUNOGLOBULIN (HORSE) Protein / enzyme biologic 1 mg/kg
Comparator Fludarabine Small molecule 30 mg/m2 Intravenous
Comparator Melphalan Small molecule 100 mg/m2 Intravenous
Comparator Sirolimus Small molecule
Comparator Tacrolimus Small molecule