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Clinical Trial Summary

This is a first-in-human, open-label, dose escalation and expansion study of UCART22 administered intravenously to patients with relapsed or refractory B-cell acute Lymphoblastic Leukemia (B-ALL). The purpose of this study is to evaluate the safety and clinical activity of UCART22 and determine the Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (RP2D)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04150497
Study type Interventional
Source Cellectis S.A.
Contact Cellectis Central Contact
Phone +1 (347) 752-4044
Email clinicaltrials@cellectis.com
Status Recruiting
Phase Phase 1
Start date October 14, 2019
Completion date January 31, 2026

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