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

Study Number

84119

Phase

Age Group

Adult

Principal Investigator

Purpose

This first-in-human (FIH) dose-escalation and dose-validation/expansion study will assess ziftomenib (KO-539), a menin-MLL(KMT2A) inhibitor, in patients with relapsed or refractory acute myeloid leukemia (AML).

Check your eligibility for this trial

Check now

Full Title

A Phase 1/2A First in Human Study of the Menin-MLL(KMT2A) Inhibitor
KO-539 in Patients with Relapsed or Refractory Acute Myeloid Leukemia

ClinicalTrials.Gov ID

NCT04067336

Get 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.