ID
13489
Description
Randomized study with a run-in dose-selection phase to assess the added value of Lenalidomide in combination with standard remission-induction chemotherapy and post-remission treatment in patients aged 18-65 years with previously untreated acute myeloid leukemia (AML) or high risk myelodysplasia (MDS) (IPSS-R risk score> 4.5) Description of Form: End of Protocol Form
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- 2/11/16 2/11/16 -
Uploaded on
February 11, 2016
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Creative Commons BY-NC 3.0
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End of Protocol Form HOVON 132 AML/SAKK 30/13 EudraCT 2013-002843-26
End of Protocol Form
- StudyEvent: ODM
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End of Protocol Form
- StudyEvent: ODM