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Clinical Trial Summary

The purpose of this study is to determine the safety and efficacy of post-transplant cyclophosphamide and a post-transplant infusion of donor cells, that have been specially processed to remove alpha beta t-cells, in patients undergoing a haploidentical allogeneic stem cell transplant to help reduce the risk of relapse without increasing the risk of graft-versus-host disease.


Clinical Trial Description

Transplant patients participating in this clinical trial will receive one of 3 standard pre-transplant chemotherapy preparative regimens as appropriate for their specific disease. They will then receive a standard non-manipulated donor stem cell infusion on transplant day (day 0) followed by cyclophosphamide (days +3 and +4) and an alpha-beta t-cell reduced donor stem cell infusion on day +7. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02193880
Study type Interventional
Source University of Alabama at Birmingham
Contact
Status Completed
Phase N/A
Start date October 9, 2014
Completion date March 13, 2018

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