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To Observe the Dual-target Chimeric Antigen Receptor T Cells in the Treatment of B Cell Hematologic Tumors

To Observe the Dual-target Chimeric Antigen Receptor T Cells in the Treatment of B Cell Hematologic Tumors

Recruiting
18-70 years
All
Phase 1

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Overview

To observe the long-term efficacy and safety of dual-target chimeric antigen receptor T cells in the treatment of refractory relapsed B cell hematologic tumors (at least 2 years).

Description

This study is open single-arm prospective clinical study To relapse/refractory blood B cell tumor patients as the subjects, according to the expression of tumor cells, gives the corresponding double targets CART cell injection treatment, follow-up observation of the adverse reactions and the treatment effect of the drug to the data (at least 2 years), assessment of double targets CAR - T Long-term efficacy and safety of cell injection

Eligibility

Inclusion Criteria:

  1. Refractory and relapsed B-cell tumor determined by clinical diagnosis, B cell tumors include the following three categories: B cell acute lymphocyte leucocyte; Inert B cell lymphoma (CLL、 FL、 MZL); Aggressive B-cell lymphoma (DLBCL、 BL、 MCL);
  2. CD19 positive and CD20 positive or CD22 positive were detected by immunohistochemistry or flow cytometry; 3.18 years old≤age≤70 years old;
        4.Estimated survival time>3 months; 5.ECOG Scores: 0~2; 6.There should be at least one
        measurable tumor foci according to RECIST Version 1.1; 7.The functions of vital organs must
        meet the following conditions: EF>50%, and no obvious abnormality of electrocardiogram;
        SpO2≥92%; Cr≤1.5ULN; ALTand AST≤5ULN, TBil≤3ULN; 8.Subjects planning to become pregnant
        must agree to use contraception prior to enrolling in the study and after six months of
        study duration; inform the investigator immediately if the subject becomes pregnant or
        suspects pregnancy; 9.The subject or guardian understands and signs the informed consent.
        Exclusion Criteria:
          1. With other diseases that are not effectively controlled, including, but not limited
             to, persistent or poorly controlled infections symptomatic congestive heart failure
             unstable angina arrhythmia poorly controlled pulmonary disease or psychiatric disease;
          2. Presence of other malignant tumors;
          3. There are severe infections that cannot be effectively controlled;
          4. Hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) positive,
             peripheral blood hepatitis B virus (HBV)DNA higher than the detection limit should be
             excluded; If hepatitis C virus (HCV) antibody positive, peripheral blood HCV RNA
             positive need to exclude; Cytomegalovirus (CMV)DNA positive; Epstein-barr virus DNA
             positive in peripheral blood;
          5. Known positive serology for human immunodeficiency virus (HIV) or syphilis;
          6. A history of severe allergies to biological products (including antibiotics);
          7. Patients with relapses after allogeneic hematopoietic stem cell transplantation with
             grade 3-4 acute graft-versus-host disease (GvHD);
          8. Female patients who are under pregnancy and/or lactation;
          9. Active autoimmune disease requiring systemic immunosuppressive therapy;
         10. Conditions that the investigator believes may increase the risk to the subject or
             interfere with the results of the study.

Study details
    19 and 22+ B Cell Hematologic Tumors
    19 and 20+ B Cell Hematologic Tumors

NCT05388695

Hebei Senlang Biotechnology Inc., Ltd.

27 January 2024

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