CD19/CD20 Dual-CAR-T for Patients With B-cell Lymphoma
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Percentage of participants with adverse events.
研究概览
简要总结
This is a single center, single arm, open-label, phase I study to evaluate the safety and efficacy of CD19/CD20 Dual-CAR-T cells in patients with refractory and relapsed B-cell lymphoma.
详细描述
This Phase I study is designed as a pilot trial evaluating the safety and efficacy of CD19/CD20 Dual-CAR-T cell therapy in subjects with refractory and relapsed B cell lymphoma. Subjects will receive cytoreductive chemotherapy with cyclophosphamide and fludarabine on days -5, -4 and -3 followed by infusion of CD19/CD20 Dual-CAR-T cells. Safety and efficacy of CD19/CD20 Dual-CAR-T cells therapy will be monitored. The purpose of current study is to determine the clinical efficacy and safety of CD19/CD20 Dual-CAR-T cells therapy in patients with refractory and relapsed B-cell lymphoma.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 1 Year 至 80 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Relapsed and refractory B-cell lymphoma with:
- •Relapsed or refractory disease after ≥2 lines of chemotherapy including rituximab and anthracycline and either having failed after autologous or allogeneic hematopoietic stem cell transplantation (ASCT);
- •Patients must have evaluable evidence of disease, including minimal residual disease (MRD);
- •Double positive expression of CD19 / CD20 in B cells;
- •Ages 1 to 80 years, including boundary values;
- •ECOG score 0-3 points;
- •Women of childbearing age (15-49 years old) must receive a pregnancy test within 7 days prior to initiation of treatment and the results are negative; male and female patients with fertility must use an effective contraceptive to ensure 3 months after discontinuation of treatment during the study period not pregnant inside;
- •Patients who voluntarily sign informed consent and are willing to comply with treatment plans.
排除标准
- •patients with organ failure:
- •Heart: NYHA heart function grade IV;
- •Liver: Grade C that achieves Child-Turcotte liver function grading;
- •Kidney: kidney failure and uremia;
- •Lung: symptoms of respiratory failure;
- •Brain: a person with a disability;
- •Active infections that are difficult to control;
- •Human immunodeficiency virus (HIV) positive;
- •Liver and kidney function: total bilirubin > 5 × ULN, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 5 × ULN, serum creatinine clearance rate 60mL / min;
- •GVHD ≥ 2 or anti-GVHD treatment;
- •intracranial hypertension or unconsciousness; respiratory failure; diffuse vascular internal coagulation;
- •pregnant or lactating women;
- •The patient does not agree to use effective contraception during the treatment period and for the next 3 months;
- •Patients who participate in other clinical studies at the same time;
- •The investigator believes that there are other factors that are not suitable for inclusion or influence the subject's participation or completion of the study.
结局指标
主要结局
Percentage of participants with adverse events.
时间窗: 6 months
Objective remission rate(ORR)
时间窗: 6 months
The percentage of participants who achieved complete remission (CR) and partial remission over all participants.
次要结局
- Relapse-Free Survival(RFS )(6 months)
- Overall-Survival(OS)(6 months)
- Persistence of CAR-T cells in vivo(6 months)