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Clinical Trial Summary

The purpose of this study is to provide data on the activity of a standard daunorubicin, cytarabine, and etoposide (ADE) induction plus epigenetic priming with decitabine as assessed by standard measures of complete remission (CR), leukemia free survival (LFS) and overall survival (OS), as well as, on minimal residual disease (MRD). It will also provide necessary data on the safety and Pharmacokinetics (PK) of decitabine in pediatric patients that is currently unavailable.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT01177540
Study type Interventional
Source Eisai Inc.
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Status Terminated
Phase Phase 2
Start date March 3, 2011
Completion date July 19, 2013