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临床试验/NCT02837757
NCT02837757终止不适用

Everolimus Modulation of Anti-tumor T CD4 Immune Responses

Centre Hospitalier Universitaire de Besancon3 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2015年11月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
14
试验地点
3
主要终点
Change in regulatory T cell counts during treatment with everolimus

研究概览

简要总结

Everolimus is an inhibitor of mammalian target of rapamycin, approved in patients with metastatic renal cell carcinoma.

The objective of this study is to investigated the influence of everolimus immune modulation on antitumor efficacy .

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • Performance status ECOG-WHO 0, 1 or 2
  • Metastatic renal cancer
  • Patient candidate to everolimus treatment
  • signed written informed consent
  • fertile women with adequate contraception during the study and until 8 weeks after stopping treatment

排除标准

  • Patients under chronic treatment with systemic corticoids or other immunosuppressive drugs (prednisone or prednisolone ≤ 10 mg/day is allowed)
  • History of immune deficiency
  • Hypersensitivity against rapamycin and derived
  • Prior history of other malignancy except for: basal cell carcinoma of the skin, cervical intra-epithelial neoplasia and other cancer curatively treated with no evidence of disease for at least 5 years
  • Active autoimmune diseases, HIV, hepatitis C or B virus
  • Patients with any medical or psychiatric condition or disease,
  • Patients under guardianship, curatorship or under the protection of justice.

结局指标

主要结局

Change in regulatory T cell counts during treatment with everolimus

时间窗: 9 months after everolimus initiation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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