drugset / Trial / NCT06434467

The Efficacy and Safety of Nelarabine Injection in Patients With T-lymphoblastic Leukemia and T-lymphoblastic Lymphoma

NCT06434467

NaSingle-groupOpen-labelTreatment

Summary

This is a single-arm, open-label, multicenter, phase III clinical study that aims to evaluate the efficacy and safety of Nelarabine injection in the treatment of refractory or recurrent T-lymphoblastic leukemia (T-ALL) and T-lymphoblastic lymphoma (T-LBL) in both children and adults. The trial includes 83 subjects, consisting of 35 adults and 48 children, and aims to evaluate the composite complete response rate (CCR) within 2 cycles, assessed by the Independent Review Committee (IRC), following treatment with Nelarabine injection for children and adults with refractory or recurrent T-ALL and T-LBL. The sample size of this study is estimated according to the treatment period of 4 cycles.

Timeline

Start
2024-05
Primary completion
2025-12
Completion
2026-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Nelarabine Small molecule 650 mg/m2 Intravenous
Subject Nelarabine Small molecule 1500 mg/m2 Intravenous