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NCT Number: NCT06355739

CD19-targeted CAR T Cell Autotransfusion for the Treatment of Recurrent/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma in Children With CD19+

To evaluate the safety and efficacy of BIC-19GG, BIC-2019, BIC-2219 in the treatment of relapsed/refractory B acute lymphoblastic leukemia/lymphoblastic lymphoma in children

Recruiting

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Key information

Age range

3 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Pediatrics, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences, Tianjin, Tianjin Municipality, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

1, age 3-18 years old (including boundary value), male and female;

  • The patient was clinically diagnosed as relapsed/refractory B acute lymphoblastic leukemia/lymphoblastic lymphoblastic

Patients with tumors who meet one of the following conditions:

  • Complete marrow response (MRD>1%) or not achieved after at least 2 courses of standardized induction regimen chemotherapy

Complete response at the molecular level and immunology (characterized by specific molecular markers and immunophenotypes prior to treatment)

Patients, did not turn negative after treatment);

  • Recurrence during chemotherapy, early recurrence after drug withdrawal (<12 months) or late recurrence after complete remission (≥

12 months) and did not achieve complete remission after 1 course of standard induction regimen (MRD>1%);

  • Recurrence after bone marrow transplantation;
  • Simple bone marrow, simple extramedullary (testicular leukemia, central nervous system leukemia) or combined

recrudescence

  • Lansky score ≥60;

4, the treatment related antigen test result is positive (CD19/CD20/CD22);

  • The expected survival period from the signing date of the informed consent is more than 3 months;

6, HGB≥70g/L (blood transfusion);

7, liver and kidney function, cardiopulmonary function meet the following requirements:

  • Creatinine ≤1.5×ULN;
  • Left ventricular ejection fraction ≥50%;
  • Blood oxygen saturation >90%;
  • Total bilirubin ≤1.5×ULN; ALT and AST≤2.5 x ULN.-

Exclusion criteria

  • 1, severe cardiac insufficiency, left ventricular ejection fraction <50%;

2, have a history of severe lung function impairment;

  • Combined with other advanced malignant tumors;

4, combined with serious infection and can not be effectively controlled;

5, combined with serious autoimmune disease or congenital immune deficiency;

6, active hepatitis (hepatitis B virus deoxyribonucleic acid [HBVDNA] or hepatitis C virus ribonucleic acid [HCVRNA] positive);

7, human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS), or syphilis infection;

  • Have a history of severe allergy to biological products (including antibiotics);
  • Patients with allogeneic hematopoietic stem cell transplantation still had acute graft-versus-host response (GvHD) one month after immunosuppressant discontinuation;

10, the presence of other serious physical or mental illnesses or abnormalities in laboratory tests that may increase the risk of participating in the study or interfere with the study results, as well as patients deemed unsuitable for participation in the study by the investigator.

Treatment and study plan

CAR T cell injection

Device

intravenous injection

Primary outcomes

  1. Overall survival and event-free survival

    Time frame: 24 months post CAR-T cell infusion

    The prognosis of ALL children who underwent CAR-T cell therapy

Secondary outcomes

  1. Overall remission rate

    Time frame: One month post CAR-T cell infusion

    The ORR of ALL children who underwent CAR-T cell therapy

  2. Adverse events

    Time frame: 12 months post CAR-T cell infusion

    Incidence of adverse events and its severity

Sponsors and collaborators

Lead sponsor

Zhu Xiaofan

Other

Registry information

Official study title

Phase II Clinical Study on the Safety and Efficacy of Autotransfusion Agents Targeting CD19 Chimeric Antigen Receptor T Lymphocytes (BIC-19GG, BIC-2019,BIC-2219)in the Treatment of CD19-positive Children With Relapsed/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Apr 9, 2024
Registry last updated
Apr 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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