RecruitingPhase 1NCT07166419

Anti-CD19/20/22 Chimeric Antigen Receptor T Cells (TriCAR19.20.22 T Cells) for the Treatment of Relapsed or Refractory Non-Hodgkin Lymphoma, Acute Lymphoblastic Leukemia, and Chronic Lymphocytic Leukemia

Phase I Clinical Trial of Caring Cross Anti-CD19/20/22 Chimeric Antigen Receptor T Cells for Treatment of Relapsed or Refractory Lymphoid Malignancies (Non-Hodgkin Lymphoma, Acute Lymphoblastic Leukemia, Chronic Lymphocytic Leukemia) (C3PO)


Sponsor

Ohio State University Comprehensive Cancer Center

Enrollment

24 participants

Start Date

Jan 14, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This phase I trial tests the safety, side effects and best dose of anti-CD19/20/22 chimeric antigen receptor (CAR) T cells (TriCAR19.20.22 T cells) and how well they work in treating patients with non-Hodgkin lymphoma, acute lymphoblastic leukemia (ALL) and chronic lymphocytic leukemia (CLL) that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). CAR T-cell therapy is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack cancer cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein, such as CD19, CD20 and CD22, on the patient's cancer cells is added to the T cells in the laboratory. The special receptor is called a CAR. Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain cancers. Giving TriCAR19.20.22 T cells may be safe, tolerable, and/or effective in treating patients with relapsed or refractory non-Hodgkin lymphoma, ALL and CLL.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing a new type of immune cell therapy called TriCAR19.20.22 T cells — engineered immune cells that are designed to recognize and attack blood cancer cells by targeting three proteins at once (CD19, CD20, and CD22). It is being studied in people with relapsed or refractory (hard-to-treat) blood cancers including non-Hodgkin lymphoma, leukemia, and chronic lymphocytic leukemia. **You may be eligible if...** - You have non-Hodgkin lymphoma, acute lymphoblastic leukemia, or chronic lymphocytic leukemia that has come back or stopped responding to treatment - You have received at least two prior lines of therapy - Prior CAR T-cell therapy targeting CD19, CD20, or CD22 is allowed - You are in sufficient health to tolerate the treatment **You may NOT be eligible if...** - You have active, uncontrolled infection - You have significant heart, lung, liver, or kidney problems - You are pregnant or breastfeeding - You have had an allogeneic stem cell transplant within the past 6 months Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALAutologous Anti-CD19/CD20/CD22 CAR T-cells

Given IV

PROCEDUREBiospecimen Collection

Undergo blood sample collection

PROCEDUREBone Marrow Aspiration

Undergo bone marrow biopsy and aspiration

PROCEDUREBone Marrow Biopsy

Undergo bone marrow biopsy and aspiration

PROCEDUREComputed Tomography

Undergo PET/CT

DRUGCyclophosphamide

Given IV

PROCEDUREEchocardiography Test

Undergo echocardiography

DRUGFludarabine

Given IV

PROCEDUREMultigated Acquisition Scan

Undergo MUGA

PROCEDUREPheresis

Undergo apheresis

PROCEDUREPositron Emission Tomography

Undergo PET/CT


Locations(1)

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

View Full Details on ClinicalTrials.gov

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NCT07166419


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