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Title   An Open-label, Multicenter Phase 1 Study to Characterize the Safety, Tolerability, Preliminary Antileukemic Activity, Pharmacokinetics, and Maximum Tolerated Dose or Pharmacological Active Dose of BAY2402234 in Patients With Advanced Myeloid Malignancies
Disease/Condition   Myelodysplastic Syndrome (MDS),Leukemia,Cancer,Neoplasms

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Eligibility Criteria   Click here for eligibility requirements
Principal Investigator   Amit Verma, MD
Contact Name   Apoorva Talanki
Contact Email
Protocol Number   18-06-93-01
Inclusion/Notes   This Information was obtained from
Status   Active/Enrolling
Adult Clinical Trial   Yes
Pediatric Clinical Trial   No
Sub-Specialty   Acute Leukemia
Adult, Pediatric, Both   Adult