drugset / Trial / NCT02746952

Dose Escalation Study of UCART19 in Adult Patients With Relapsed / Refractory B-cell Acute Lymphoblastic Leukaemia

NCT02746952 ↗

Phase 1 Completed 25 enrolled Servier ADIR, a Servier Group company · collab
NaSingle-groupOpen-labelTreatment

Summary

The study is in two parts: a dose escalation then a safety dose expansion. The purpose of the dose escalation part is to evaluate the safety and tolerability of ascending doses of UCART19 (dose-escalation part) given as a single infusion in patients with relapsed / refractory (R/R) B-cell acute lymphoblastic leukaemia (B-ALL), to determine the maximum tolerated dose (MTD), the recommended dose and the lymphodepletion regimen. The purpose of the safety dose expansion is to assess the safety and tolerability of the RD for UCART19.

Timeline

Start
2016-08-01
Primary completion
2020-07-28
Completion
2020-07-28

Drugs

EvaluationDrugModalityDoseRoute
Subject UCART19 Cell therapy 6e+06 cells Intravenous
Subject UCART19 Cell therapy 6e+07 cells Intravenous
Subject UCART19 Cell therapy 1.8e+08 cells Intravenous