This is a multicenter (S. Korea/US), Phase Ib, open-label, dose-finding study to assess safety, PK, PD, and preliminary efficacy of CWP232291 administered in combination with ara-C in subjects with relapsed or refractory AML. Based on the poor prognosis of relapsed/refractory AML, exploration of alternative doses and regimens will be evaluated and approved by a Safety Review Committee (SRC).
*For Eligibility information, look up the trial at NIH by clicking on the Study Number above.*
Other eligibility criteria may apply.
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