In VIVO CAR-T Therapy for Relapsed/Refractory Hematological Malignancies

Официальное название

Intracellularly Prepared Chimeric Antigen Receptor T-cell Therapy Targeting CD19 for the Treatment of Relapsed/Refractory Hematological Malignancies

Обзор

This study is an investigator-initiated single center, single arm clinical study with a target population of patients with relapsed or refractory malignant hematological tumors. It is an early exploratory clinical study of the safety, tolerability and initial efficacy in the treatment of relapsed or refractory malignant hematological tumors.

Подробное описание

This is an open-label, single-arm study to evaluate the efficacy and safety of in vivo Chimeric Antigen Receptor T-Cell(CAR-T cell) therapy in patients with relapsed refractory malignant hematological tumors. Upon enrollment, subjects will receive an intravenous infusion of the in Vivo CAR-T preparation. Following the infusion, subjects will be hospitalized for observation, and subjects will be evaluated for safety and efficacy. Subjects will be followed for up to 2 years to determine if the disease is under control.

Вмешательства

• Биопрепарат Invivo CAR-T
  Patients were enrolled and given a single dose of CAR-T injection intravenously, hospitalized for observation over the following month, and followed up for observation over the following 2 years.

Первичные конечные точки

• Maximal Tolerated Dose(MTD) [Срок оценки: Up to 28 days after infusion]
• Incidence of adverse events(AE) after infusion [Срок оценки: Up to 28 days after infusion]

Вторичные конечные точки (1)

• Objective Response Rate [Срок оценки: Day 28、Month 2、Month 3、Month 6、Month 12、Month 18、Month 24]

Критерии участия

Критерии включения

• Age ≥ 18 years old, gender unrestricted;
• Confirmed diagnosis of relapsed/refractory malignant hematological tumors, including B-ALL, B-cell lymphoma and multiple myeloma;
• ECOG performance status score 0-2, with an expected survival period of ≥ 3 months;
• Blood routine test results during the screening period meet the following criteria:

① Hemoglobin ≥ 6 g/dL (no red blood cell transfusion within 1 week before screening), recombinant human erythropoietin (rhEPO) is allowed; for patients meeting the hemoglobin ≥ 6 g/dL criterion, red blood cell transfusion can be used to maintain hemoglobin ≥ 6 g/dL;

• Absolute neutrophil count (ANC) ≥ 600/μL (no use of granulocyte colony-stimulating factor \[G-CSF\] within 1 week before screening, or no use of pegylated G-CSF within 2 weeks before screening); ③ Platelet count ≥ 50,000/μL; ④ Lymphocyte count ≥ 500/μL;
• Normal renal function during the screening period: creatinine clearance rate (CrCl) ≥ 45 mL/min (calculated using the Cockcroft-Gault formula);
• Liver function during the screening period meets the following criteria:

① Alanine aminotransferase (ALT), aspartate aminotransferase (AST) ≤ 3.0 × ULN;

② Total bilirubin (TBIL) ≤ 2.0 × ULN (except for congenital hyperbilirubinemia such as Gilbert's syndrome, direct bilirubin can be relaxed to ≤ 1.5 × ULN);

• Cardiac function during the screening period meets the following criteria:

① Left ventricular ejection fraction (LVEF) ≥ 40% (measured by echocardiography or MUGA scan);

② No clinically significant pericardial effusion;

③ No clinically significant electrocardiogram (ECG) abnormalities;

• Pulmonary function during the screening period meets the following criteria: blood oxygen saturation (SpO₂) ≥ 90%;
• Women of childbearing age must have a negative pregnancy test during the screening period and before drug administration, and must not be in the lactation period;
• Men and women of childbearing age must agree to take effective contraceptive measures and not donate reproductive cells (including sperm or eggs) from the time of signing the informed consent form until 1 year after the end of study drug administration;
• The subject or their legally authorized representative has signed the informed consent form (ICF), indicating their understanding of the purpose and procedures of the study and their voluntary participation in this study.

Критерии исключения

• Other anti-tumor treatments within the screening period (judged by the investigator comprehensively):

① Received chemotherapy, targeted therapy or immunotherapy within 5 half-lives before administration;

② Received radiotherapy within 4 weeks before administration (if the radiotherapy target area covers ≤ 5% of bone marrow reserve, the time limit for radiotherapy completion is not restricted);

• History of hematopoietic stem cell transplantation: Received allogeneic or autologous hematopoietic stem cell transplantation within 3 months before administration;
• History of other malignant tumors (except for this disease), except for the following situations:

① Received radical treatment and had no known active disease for ≥ 2 years before enrollment;

② Had fully treated non-melanoma skin cancer in the past and had no active lesions at present;

• Received treatment related to vesicular stomatitis virus glycoprotein (VSVG) pseudotyped virus in the past;
• Had severe and uncontrolled infections (bacterial, viral, fungal, etc.) within the screening period;
• Clinically significant cardiac diseases:

• Had symptomatic heart failure or other serious cardiac diseases (such as severe arrhythmia);

• Had New York Heart Association (NYHA) Class III-IV congestive heart failure; ③ Had a myocardial infarction or received coronary artery bypass grafting (CABG) / coronary artery stent implantation within 6 months before signing the informed consent;

• Had clinically significant ventricular arrhythmia or a history of unexplained syncope; ⑤ Had a history of syncope (excluding cases caused by vasovagal reactions or dehydration); ⑥ Had a history of severe non-ischemic cardiomyopathy;
• Other clinically significant diseases, including but not limited to:

• Primary immunodeficiency; ② Had a stroke or seizure within 6 months before screening;

• Had clear clinical evidence of dementia or mental status changes; ④ Had Parkinson's disease, Parkinson-like movement disorders or a history of the above;
• Had undergone surgery within 2 weeks before administration, or planned to undergo surgery within 2 weeks after administration (local anesthesia surgery excluded);
• Had received live attenuated vaccines within 1 month before administration;
• Had a history of severe allergic reactions to this product or its formulation components;
• Patients who were not suitable for establishing intravenous access;
• The investigator believed that there were other conditions that made the patient unsuitable for participating in this study.

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 · 1 центр

• 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China — Куньмин

Идентификаторы

NCT: NCT07239323 · PBC027-1

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗