drugset / Trial / NCT02228096

Study of Efficacy and Safety of CTL019 in Pediatric ALL Patients

NCT02228096

Phase 2 Completed 75 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This was a single arm, open-label, multi-center, phase II study to determine the efficacy and safety of an experimental therapy called CTL019 T-cells in pediatric patients with B-cell acute lymphoblastic leukemia, who were refractory to standard chemotherapy regimen or relapsed after allogeneic stem cell transplant.

Timeline

Start
2014-08-14
Primary completion
2018-05-29
Completion
2019-05-24

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tisagenlecleucel Cell therapy 200000 cells/kg
Subject Tisagenlecleucel Cell therapy 2e+06 cells/kg
Subject Tisagenlecleucel Cell therapy 5e+06 cells/kg
Subject Tisagenlecleucel Cell therapy 1e+07 cells
Subject Tisagenlecleucel Cell therapy 1e+08 cells
Subject Tisagenlecleucel Cell therapy 2.5e+08 cells