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Study identifier: NCT04113616 Synced from ClinicalTrials.gov · July 28, 2026
● Terminated

An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 When Administered Alone and in Combination With Low-Dose Cytarabine (LDAC) or Decitabine in Patients With Acute Myeloid Leukemia (AML)

Condition: Relapsed or Refractory Acute Myeloid Leukemia (AML) · Acute Myeloid Leukemia (AML), Secondary to Myeloproliferative Neoplasms (MPN)  ·  Sponsor: Kartos Therapeutics, Inc.

PhasePhase 1/Phase 2
Planned participants70
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study evaluates KRT-232, a novel oral small molecule inhibitor of MDM2, when administered alone and in combination with low-dose cytarabine (LDAC) or Decitabine for the treatment of adults with Acute Myeloid Leukemia (AML) and AML secondary to myeloproliferative neoplasms (MPN). Participants must be relapsed/refractory (having failed prior therapy) and will be assigned to receive monotherapy (KRT-232 alone) or combination therapy (KRT-232 with LDAC or KRT-232 with Decitabine).

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

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Locations (59)

University of ChicagoChicago, Illinois, United States
University of Maryland Medical CenterBaltimore, Maryland, United States
Mount SinaiNew York, New York, United States
Memorial Sloan Kettering Cancer CenterNew York, New York, United States
Weill CornellNew York, New York, United States
The Ohio State UniversityColumbus, Ohio, United States
Oregon Health and Science UniversityPortland, Oregon, United States
MD Anderson Cancer CenterHouston, Texas, United States
Monash HealthClayton, Australia
St. George HospitalKogarah, Australia
Royal Perth HospitalPerth, Australia
Calvary Mater Newcastle HospitalWaratah, Australia

+ 47 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT04113616