RecruitingNCT02161783

Treatment of Graft Failure After Hematopoietic Stem Cell Transplantation


Sponsor

Masonic Cancer Center, University of Minnesota

Enrollment

50 participants

Start Date

Oct 6, 2014

Study Type

OBSERVATIONAL

Conditions

Summary

This is a guideline for the treatment of graft failure after hematopoietic stem cell transplant (HSCT). This regimen, consisting of cyclophosphamide and fludarabine with low dose total body irradiation (TBI) is designed to promote donor engraftment by day 42 after initial graft failure. The graft will consist of bone marrow or G-CSF mobilized peripheral blood from a haploidentical related donor. The source of stem cells will be determined by the transplant team based on factors such as patient's age, medical history, donor availability and will be according to the current University of Minnesota Blood and Marrow Transplantation Program selection guidelines.


Eligibility

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Cyclophosphamide, a drug called Fludarabine, and others for people with secondary graft failure and primary graft failure. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFludarabine

Fludarabine 30 mg/m2 IV over 1 hour given on days -6 through -2 of transplant.

DRUGCyclophosphamide

Cyclophosphamide 14.5 mg/kg IV over 1-2 hours given on days -6 and -5 from transplant. And Cyclophosphamide 50 mg/kg IV over 2 hours given on days +3 and +4 from transplant.

RADIATIONTotal Body Irradiation

TBI 200cGy in a single fraction on day -1 from transplant.

BIOLOGICALHematopoietic stem cell infusion

Hematopoietic stem cell infusion given on day 0.


Locations(1)

University of Minnesota Medical Center, Fairview

Minneapolis, Minnesota, United States

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NCT02161783


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