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)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT06466395


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