RecruitingPhase 1NCT06466395
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
Sponsor
M.D. Anderson Cancer Center
Enrollment
22 participants
Start Date
Feb 18, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
To find the recommended dose of hyper-CVAD in combination with venetoclax that can be given to participants with relapsed or refractory leukemia.
Eligibility
Min Age: 2 YearsMax Age: 21 Years
Plain Language Summary
Simplified for easier understanding
This phase I study is testing the safety of a chemotherapy combination called Hyper-CVAD together with venetoclax in children, teenagers, and young adults with relapsed or treatment-resistant acute lymphoid leukemia (a blood cancer) that has come back or failed to respond to previous therapies.
**You may be eligible if...**
- You are a pediatric, adolescent, or young adult patient
- You have relapsed or refractory acute leukemia of the lymphoid type (including bi-phenotypic or undifferentiated leukemia)
- At least 5% of your bone marrow or blood consists of leukemia cells
**You may NOT be eligible if...**
- Your leukemia is of a different type (e.g., purely myeloid)
- You have serious organ problems that prevent safe treatment with intensive chemotherapy
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DRUGVenetoclax
Given by PO
DRUGHyper-CVAD
Given by IV
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06466395
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