drugset / Trial / NCT05075681

Ruxolitinib and Chidamide for Acute T Cell Lymphoblast Leukemia/ Lymphoblastic Lymphoma

NCT05075681

Phase 1/2 Unknown 50 enrolled Chinese PLA General Hospital
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the efficacy and safety of Ruxolitinib and Chidamide intensified conditioning regimen in patients with Acute T cell Lymphoblast leukemia/ lymphoblastic lymphoma Underwenting Haploidenticl Peripheral blood Stem Cell Transplantation.

Timeline

Start
2021-11-01
Primary completion
2024-06-01
Completion
2025-06-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 35 mg Oral
Subject Tucidinostat Small molecule 30 mg
Background Busulfan Small molecule 0.8 mg/kg Intravenous
Background Cyclophosphamide Other / unclassified 1800 mg/m2
Background Cytarabine Small molecule 4000 mg/m2
Background carmustine Small molecule 250 mg/m2 Intravenous