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Clinical Trial Summary

Given the increased number of HLA-mismatched haploidentical transplantation with post-transplant cyclophosphamide performed each year and the high risk of infectious complications associated with this type of transplant, the investigators suggest that GM-CSF administration post-infusion of T-replete haploidentical stem cells and post-transplant cyclophosphamide can yield similar count recovery rates to G-CSF with a potential of lowering risk of infectious complications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04237623
Study type Interventional
Source Northside Hospital, Inc.
Contact Stacey Brown, BA
Phone 404-780-7965
Email stacey.brown@northside.com
Status Recruiting
Phase Phase 2
Start date May 18, 2020
Completion date September 18, 2025

See also
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Completed NCT03434704 - Peripheral Blood Stem Cell Transplantation From Family Haploidentical Donors in Patients With Myelodysplastic Syndrome and Acute Leukemia Under Primary Prophylaxis With Posaconazole Phase 2
Withdrawn NCT01751243 - Transplantation of Hematopoietic Progenitors From Haploidentical Donor With Selective in Vitro Depletion Allo-reactive Lymphocytes in Patient With High Risk Hematological Malignancies Phase 1
Terminated NCT03963024 - Treosulfan-TMI Conditioning and Rapamycin GvHD Prophylaxis Before Allo-HSCT Phase 1
Completed NCT03961919 - Phase II Trial in Elderly Patients With AML or MDS in Complete Remission Not Eligible for Allogenic Transplant Phase 2