drugset / Trial / NCT01626092

Reduced-Intensity Hematopoietic Stem Cell Transplant for High Risk Lysosomal and Peroxisomal Disorders

NCT01626092

NaSingle-groupOpen-labelTreatment

Summary

This study is designed to test the ability to achieve donor hematopoietic engraftment while maintaining low rates of transplant-related mortality (TRM) in patients with high-risk lysosomal and peroxisomal disorders using a novel conditioning regimen for hematopoietic cell transplantation (HCT). After a reduced-intensity conditioning regimen using volumetric-modulated arc therapy (VMAT)-delivered low-dose total body irradiation (TBI) with highly conformal marrow boosting, patients will be transplanted using either a related or unrelated allograft. The cell source may be marrow, peripheral blood or cord blood based on donor availability.

Timeline

Start
2012-07-11
Primary completion
2013-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Background Alemtuzumab Monoclonal antibody 0.3 mg/kg Intravenous
Background Clofarabine Other / unclassified 40 mg/m2 Intravenous
Background Cyclosporine Peptide 2.5 mg/kg Intravenous
Background Melphalan Small molecule 140 mg/m2 Intravenous
Background Mycophenolate Mofetil Small molecule 15 mg/kg Oral
Background Mycophenolate Mofetil Small molecule 1 g Oral