First in Human Study of KO-539 in Relapsed or Refractory Acute Myeloid Leukemia
Study Number: 

P 84119

Phase: 
1
Principal Investigator: 
Eunice Wang, MD

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Official Title: 
(KO-MEN-001) A Phase 1 First in Human Study of the Menin-MLL(KMT2A) Inhibitor KO 539 in Patients with Relapsed or Refractory Acute Myeloid Leukemia
Purpose: 
This first-in-human (FIH) dose escalation will determine the maximum tolerated dose (MTD) of KO-539, a menin-MLL(KMT2A) inhibitor, in patients with refractory or relapsed AML who have failed or are ineligible for any approved standard of care therapies, including HSCT.
ClinicalTrials.Gov ID: 
NCT04067336
Learn more information and eligibility criteria for this trial at ClinicalTrials.gov

To inquire about participating in these studies, call 1-800-ROSWELL (1-800-767-9355) or e-mail askroswell@roswellpark.org.