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Clinical Trial Summary

To evaluate engraftment and toxicity of a reduced intensity preparative regimen for patients who receive a matched related or unrelated donor allogeneic stem cell transplant (ASCT) for malignant hematological diseases


Clinical Trial Description

Primary Endpoints:

1. Engraftment of donor cells

2. Regimen related toxicities

Secondary Endpoints:

1. Disease-free survival

2. Overall survival ;


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00582894
Study type Interventional
Source University of Oklahoma
Contact
Status Completed
Phase N/A
Start date February 2005
Completion date March 2008

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