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Clinical Trial Summary

First-in-human, open-label, dose-finding and dose-expansion study of UCART20x22 administered intravenously in subjects with relapsed or refractory B-Cell Non-Hodgkin Lymphoma (B-NHL). The purpose of this study is to evaluate the safety and clinical activity of UCART20x22 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 NCT05607420
Study type Interventional
Source Cellectis S.A.
Contact Cellectis Central Contact
Phone +1 917 580-1088
Email clinicaltrials@cellectis.com
Status Recruiting
Phase Phase 1/Phase 2
Start date November 1, 2022
Completion date November 2027