ClinicalTrials.gov record
Recruiting Phase 1Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT04150497

Public ClinicalTrials.gov record NCT04150497. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 30, 2026, 4:38 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official 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 refractoryCD22+ B-cell Acute Lymphoblastic Leukemia (B-ALL)

Study identification

NCT ID
NCT04150497
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Cellectis S.A.
Industry
Enrollment
52 participants

Conditions and interventions

Interventions

  • CLLS52 Biological
  • UCART22 Biological

Biological

Eligibility (public fields only)

Age range
15 Years to 50 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 13, 2019
Primary completion
Jun 29, 2026
Completion
Jun 29, 2026
Last update posted
Sep 8, 2025

2019 – 2026

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
University of California, Los Angeles (UCLA) - Medical Center Los Angeles California 90095 Recruiting
University of Colorado - Aurora Cancer Center Aurora Colorado 80045 Recruiting
Sarah Cannon - Colorado Blood Cancer Institute Denver Colorado 80218 Recruiting
University of Chicago Chicago Illinois 60647 Recruiting
Dana Farber Cancer Institute Boston Massachusetts 02215 Recruiting
Roswell Park Comprehensive Cancer Center Buffalo New York 14263 Recruiting
Memorial Sloan Kettering Cancer Center (MSKCC) David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center New York New York 10021 Recruiting
Weill Medical College of Cornell University New York New York 10065 Withdrawn
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 Recruiting
Sarah Cannon - HCA Research Institute Nashville Tennessee 37203 Recruiting
Sarah Cannon - St. David's South Austin Medical Center Austin Texas 78704 Recruiting
MD Anderson Cancer Center Houston Texas 77030 Recruiting
Sarah Cannon - Texas Transplant Institute at Methodist Hospital San Antonio Texas 78229 Recruiting
University of Wisconsin Carbone Cancer Center Madison Wisconsin 53792 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04150497, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 8, 2025 · Synced Apr 30, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04150497 live on ClinicalTrials.gov.

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