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Clinical Trial Summary

This study is designed to estimate the efficacy and toxicity of familial HLA mismatched bone marrow transplants in patients with non-malignant disease who are less than 21 years of age and could benefit from the procedure.


Clinical Trial Description

Patients < 21 years of age with a non-malignant disorder benefited by hematopoietic stem cell transplant will receive a reduced intensity conditioning regimen consisting of hydroxyurea, alemtuzumab, fludarabine, thiotepa, and melphalan. This will be followed by a familial HLA-mismatched bone marrow transplant. The primary objective is to establish safety and donor cell engraftment at 100 days and 1 year post-transplant. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03128996
Study type Interventional
Source Washington University School of Medicine
Contact Shalini Shenoy, MD
Phone 314-454-6018
Email shalinishenoy@wustl.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date March 20, 2017
Completion date April 2026

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