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临床试验/NCT04012892
NCT04012892Unknown1 期

Study Evaluating the Efficacy and Safety With CD19CAR-T for Relapsed or Refractory Non-Hodgkin Lymphoma

Chinese PLA General Hospital1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2019年5月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
发起方
入组人数
12
试验地点
1
主要终点
recovery rate of patients being treated with CD19CAR-T

研究概览

简要总结

This study is a single-arm, open label, phase I clinical trial to evaluate the safety and feasibility of CD19CAR-T in treatment of relapsed / refractory non-hodgkin 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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis with Relapsed or refractory Non Hodgkin Lymphoma with CD19 positive
  • Age 18 to 65 years old, both male and female;
  • Is expected to survive more than 12 weeks;
  • Physical condition is good: 0-1 score ECOG score;
  • No obvious abnormal heart, liver, kidney, no large wounds that haven't healed on the body;
  • Into groups to participate in voluntarily, good adherence, can cooperate test observation, childbearing age women must be 7 days before starting treatment expert pregnancy test and the results were negative, and signed a written informed consent form.

排除标准

  • Organ failure, such as heart: Class III and IV; liver: to Child grading of liver function grade C; kidney: kidney failure and uremia stage; lung: symptoms of severe respiratory failure; brain: disorder of consciousness;
  • Existing serious acute infection, uncontrollable, or have fester sex and chronic infection, wound in delay no more;
  • Pregnancy and lactation women;
  • Patients who have participated in other clinical trials or other clinical trials in the past 30 days;
  • The Investigator believe the patients should not participate in this experiment.

研究组 & 干预措施

study group

Experimental

After 6 days of pre-chemotherapy, patients in study group will be injected with CD19CART cell at the dose of 5×10^4 cells/kg in 36-96 hours

干预措施: CD19 CART (Combination Product)

结局指标

主要结局

recovery rate of patients being treated with CD19CAR-T

时间窗: 6 months

the recovery rate of patients consists of complete recovery rate and partial recovery rate of patients being treated with CD19 CAR-T

次要结局

未报告次要终点

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Li Yu

Professor

Chinese PLA General Hospital

研究点 (1)

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