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

Официальное название

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

Обзор

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

Вмешательства

• Устройство CAR T cell injection
  intravenous injection

Первичные конечные точки

• Overall survival and event-free survival [Срок оценки: 24 months post CAR-T cell infusion]

Вторичные конечные точки (2)

• Overall remission rate [Срок оценки: One month post CAR-T cell infusion]
• Adverse events [Срок оценки: 12 months post CAR-T cell infusion]

Критерии участия

Критерии включения

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

2\. 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

3\. Lansky score ≥60;

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

5\. 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.-

Критерии исключения

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

2, have a history of severe lung function impairment;

3\. 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;

8\. Have a history of severe allergy to biological products (including antibiotics);

9\. 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.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Китай · 2 центра

• Department of Pediatrics, Institute of Hematology and Blood Disease Hospital, Chinese Acad — Тяньцзинь
• InstituteHBDH — Тяньцзинь

Идентификаторы

NCT: NCT06355739 · BIC-19GG, BIC-2019,BIC-2219

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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