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Study identifier: NCT06466395 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Phase I Study of Hyper-CVAD In Combination With Venetoclax In Pediatric Patients With Relapsed or Refractory Acute Leukemias That Are of the Lymphoid Lineage Including Bi-Phenotypic or Undifferentiated Leukemias

Condition: Refractory Acute Leukemia · Relapsed Acute Leukemia · Undifferentiated Leukemia  ·  Sponsor: M.D. Anderson Cancer Center

PhasePhase 1
Planned participants22
Who can joinAll sexes, 2 Years to 21 Years
Healthy volunteersNo

About this study

To find the recommended dose of hyper-CVAD in combination with venetoclax that can be given to participants with relapsed or refractory leukemia.

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

Talk to the study team

David McCall, MD  ·  (713) 792-6604  ·  dmccall1@mdanderson.org

Always discuss trial participation with your own doctor first.

Locations (1)

MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06466395