CD19.20.22 CAR T-cells for Patients With Relapsed/Refractory B-Cell Lymphomas
NCT07168486 · Status: ENROLLING_BY_INVITATION · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 15
Last updated 2025-09-11
Summary
The goal of this study is to treat patients diagnosed with relapsed or refractory positive B cell lymphoma - positive for 2 or more target antigens - with CAR19.20.22 CAR T-cells.
Based on the preclinical characteristics of the LTG2950, CAR19.20.22 tri-specific CAR T-cells the Investigators have developed the following hypotheses to be tested in our phase Ia clinical trial. The Investigators hypothesize that these novel CAR T-cells will show:
* good safety and tolerability
* a high degree of efficacy
* very good persistence
* an acceptable level of exhaustion
Conditions
- B-Cell Lymphoma
- Diffuse Large B Cell Lymphoma (DLBCL)
- Primary Mediastinal Large B-cell Lymphoma (PMBCL)
- Follicular Lymphoma
- Transformed Follicular Lymphoma (tFL)
- Mantle Cell Lymphoma
- Chronic Lymphocytic Leukemia
- Small Lymphocytic Lymphoma
- Richter Transformation
- Marginal Zone Lymphoma
Interventions
- BIOLOGICAL
-
CD19.20.22 CAR T cells
CAR19.20.22 is a type of immunotherapy known as a chimeric antigen receptor T-cells (CAR T-cells).
- DRUG
-
Fludarabine and Cyclophosphamide
Lymphodepletion with Flu-Cy prior to CAR T cell therapy
Sponsors & Collaborators
-
University of Maryland, Baltimore
lead OTHER
Principal Investigators
-
Djordje Atanackovic, MD · Professor of Medicine
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-10-28
- Primary Completion
- 2027-07-01
- Completion
- 2028-07-01
- FDA Drug
- Yes
Countries
- United States
Study Locations
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