Phase 1/2 Study of UCART22 in Patients With Relapsed or Refractory CD22+ B-cell Acute Lymphoblastic Leukemia (BALLI-01)

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

OPEN LABEL DOSE-ESCALATION AND DOSE EXPANSION STUDY TO EVALUATE THE SAFETY, EXPANSION, PERSISTENCE AND CLINICAL ACTIVITY OF UCART22 {ALLOGENEIC ENGINEERED T-CELLS EXPRESSING ANTI-CD22 CHIMERIC ANTIGEN RECEPTOR) IN PATIENTS WITH RELAPSED OR REFRACTORY CD22+ B CELL ACUTE LYMPHOBLASTIC LEUKEMIA (B-ALL)

Intervention/treatment:
UCART22 / CLLS52
Medical condition:
B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA
Protocol code:
UCART22_01
Control number:
500871
Status:
Recruiting
Approved:
May 28, 2026
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT04150497
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
15 Years to 50 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Cellectis Central Contact
Role
CONTACT
Phone:
+1 (347) 752-4044
Sponsor
CELLECTIS S.A.
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