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Study identifier: NCT06376162 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Ziftomenib in Combination With Chemotherapy for Children With Relapsed/Refractory Acute Leukemia

Condition: Relapsed/Refractory KMT2A-r Acute Leukemia · Relapsed/Refractory NUP98-r Acute Leukemia · Relapsed/Refractory NPM1-m Acute Leukemia  ·  Sponsor: PedAL BCU, LLC

PhasePhase 1
Planned participants20
Who can joinAll sexes, 0 Years to 21 Years
Healthy volunteersNo

About this study

The primary objective of the study is to determine the recommended phase 2 dose (RP2D) of ziftomenib in combination with chemotherapy (FLA) in children with relapsed or refractory KMT2A-r, NUP98-r, or NPM1-m acute leukemia based on safety and pharmacokinetics (PK).

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

Talk to the study team

Dr. Branko Cuglievan  ·  (713) 563-1499  ·  bcuglievan@mdanderson.org

Dr. Sarah Tasian, MD  ·  (215) 590-2299  ·  tasians@chop.edu

Always discuss trial participation with your own doctor first.

Locations (20)

Children's Hospital Los AngelesLos Angeles, California, United StatesRecruiting
Children's Hospital ColoradoAurora, Colorado, United StatesRecruiting
Children's Healthcare of AtlantaAtlanta, Georgia, United StatesRecruiting
Ann & Robert H. Lurie Children's Hospital of ChicagoChicago, Illinois, United StatesRecruiting
Dana-Farber Cancer InstituteBoston, Massachusetts, United StatesRecruiting
Memorial Sloan Kettering Cancer Center - New YorkNew York, New York, United StatesRecruiting
Cincinnati Children's Hospital Medical CenterCincinnati, Ohio, United StatesRecruiting
Children's Hospital of PhiladelphiaPhiladelphia, Pennsylvania, United StatesRecruiting
St. Jude Children's Research HospitalMemphis, Tennessee, United StatesRecruiting
Texas Children's HospitalHouston, Texas, United StatesRecruiting
Seattle Children's HospitalSeattle, Washington, United StatesRecruiting
Sankt Anna-KinderspitalVienna, State of Vienna, AustriaRecruiting

+ 8 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06376162