drugset / Trial / NCT01366612

Fludarabine and Busulfan vs. Fludarabine, Busulfan and Total Body Irradiation

NCT01366612

Phase 3 Terminated 53 enrolled Hackensack Meridian Health
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a single institution study of fludarabine and busulfan versus fludarabine, busulfan and low dose total body irradiation in patients undergoing allogeneic stem cell transplantation. A study population of 80 subjects will be enrolled from The John Theurer Cancer Center at Hackensack University Medical Center. Subjects who are eligible to receive allogeneic hematopoietic stem cell transplantation according to the eligibility criteria will be consented and enrolled. Subjects will be randomly assigned to receive one of 2 conditioning regimen: fludarabine and busulfan, or fludarabine busulfan and low dose total body irradiation (TBI). Subjects will be followed until 1 year post transplantation to assess the relapse rate in each arm and transplant-related toxicity. The combination of fludarabine and busulfan is the current standard of care for patients with myeloid malignancies (AML, CML and other myeloproliferative disorders, or MDS) undergoing allogeneic transplantation at HUMC. In this study we will be comparing in a randomized fashion the standard regimen to a regimen of fludarabine, busulfan and TBI.

Timeline

Start
2010-06-16
Primary completion
2020-08-17
Completion
2020-08-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Busulfan Small molecule 130 mg/m2
Comparator Fludarabine Small molecule 40 mg/m2
Comparator rATG Unknown