Decitabine, Cytarabine, GCSF for Refractory AML/MDS

Clinical Trial Description

The primary objective of this study is to determine the feasibility and toxicity of decitabine, ARA-C and G-CSF for patients with myelodysplasia, refractory acute leukemia and poor performance status acute leukemia. ;

Study Design

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NCT number	NCT00740181
Study type	Interventional
Source	Brown University
Contact
Status	Terminated
Phase	Phase 2
Start date	August 2008
Completion date	April 2010

Decitabine, Cytarabine, GCSF for Refractory AML/MDS

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms