drugset / Trial / NCT01749293

Partially HLA Mismatched (Haploidentical) Allogeneic Bone Marrow Transplantation

NCT01749293 ↗

Phase 2 Terminated 3 enrolled University of Illinois at Chicago
NaSingle-groupOpen-labelTreatment

Summary

Allogeneic stem cell transplantation is a potentially curative treatment for patients with many hematologic malignancies (e.g. leukemia, lymphoma, and myeloma with high risk of relapse). This process requires a suitable donor. The best case scenario involves an Human Leukocyte Antigen (HLA) matched sibling donor. However, this type of donor is not always available. Donor registries can provide another source for matched unrelated donors, but this may take valuable time delaying treatment for the transplant recipient. Donor availability remains a significant barrier to the use of allogeneic (from a donor) stem cell transplant. This issue disproportionately affects patients of minority backgrounds. Novel strategies to improve outcomes using alternative donors are desperately needed. Haploidentical transplants are an alternative which provides a readily available donor in the form of a partially HLA matched family member. This provides for more potential donors and the donors can be selected based on other factors that can play a role in transplant success (e.g. age, gender, KIR alloreactivity). Recent advances in transplant techniques have greatly improved success rates with haploidentical transplants although disease relapse has remained as issue. This trial aims to provide an alternative transplant option for patients with hematologic malignancies who require bone marrow transplantation but lack an HLA identical donor. The investigational component of this study is the combination of the Fludarabine/ Busulfan/ Total Body Irradiation conditioning regimen and the HLA Haploidentical Transplant with post-transplant Cyclophosphamide.

Timeline

Start
2012-08-30
Primary completion
2014-05-15
Completion
2014-05-15

Outcome

Outcome not reported

Stopped: “The protocol design is being reconfigured in order to open a new study.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Busulfan Small molecule 6.4 mg/kg —
Subject Cyclophosphamide Other / unclassified 50 mg/kg Intravenous
Subject Fludarabine Small molecule 30 mg/m2 Intravenous