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Clinical Trial Summary

Determine the efficiency of a myéloablative conditioning associating Fludarabine, Thymoglobuline, and intravenous Busulfan with adapted dose, according to a pharmacokinetics realized in the first day of administration (or J-6 of the conditioning) of the busulfan, in preparation for a allogenic transplant family or not family compatible HLA.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02483325
Study type Interventional
Source Institut Paoli-Calmettes
Contact
Status Completed
Phase Phase 2
Start date September 2014
Completion date March 2020

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