drugset / Trial / NCT06466395

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

NCT06466395 ↗

Phase 1 Recruiting 22 enrolled M.D. Anderson Cancer Center
Non-randomizedSingle-groupOpen-labelTreatment

Summary

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

Timeline

Start
2025-02-18
Primary completion
2027-12-31
Completion
2031-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Venetoclax Small molecule — Oral