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临床试验/NCT03882840
NCT03882840招募中1 期

Induced-T Cell Like NK Cellular Immunotherapy for Cancers That Are Lack of MHC-I Expression

Second Affiliated Hospital of Guangzhou Medical University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
The safety and tolerance of the ITNK cell immunotherapy

研究概览

简要总结

T effector cells and NK cells have mutual compensatory killing functions on various of cancer types. For those cancers that have no available targets for CAR-T cell generations, we established potent T cell-like NK cells (ITNK) with a specific conversion protocol for the T cells from the patient, to perform anti-cancer therapy, especially for those cancers that are lack of MHC-I molecule expression. We have finished pre-clinical investigations for the ITNK or CAR-ITNK cell therapy and scheduled to start a clinical phase I study.

详细描述

One gene can be knockout of the T cells to produce a T-like NK cells which obtain killing function of both T effector cells and NK cells. We will collect appropriate patient's T cells, produce T-like NK cells (ITNK), and infuse the ITNK/CAR-ITNK cells back to the patients to treat various of cancers.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with advanced cancer, which express low or no MHC-I.
  • Life expectancy >12 weeks
  • Adequate heart,lung,liver,kidney function
  • Available autologous T cells
  • Informed consent explained to, understood by and signed by patient/guardian.
  • Patient/guardian given copy of informed consent.

排除标准

  • Had accepted gene therapy before;
  • Severe virus infection such as HBV,HCV,HIV,et al
  • Known HIV positivity
  • History of liver or other organ transplantation
  • Active infectious disease related to bacteria, virus,fungi,et al
  • Other severe diseases that the investigators consider not appropriate;
  • Pregnant or lactating women
  • Systemic steroid treatment (greater than or equal to 0.5 mg prednisone equivalent/kg/day)
  • Other conditions that the investigators consider not appropriate.

结局指标

主要结局

The safety and tolerance of the ITNK cell immunotherapy

时间窗: 2 years

A dose limiting toxicity is defined as any toxicity that is considered to be primarily related to the ITNK cells, which is irreversible, or life threatening or hematologic or non-hematologic Grade 3-5. Incidence of treatment-emergent adverse events will be calculated as standard methods.

次要结局

  • Percent of Patients with best response as either complete remission or partial remission.(2 years)

研究者

发起方
Second Affiliated Hospital of Guangzhou Medical University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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