跳至主要内容
临床试验/EUCTR2010-023457-11-BE
EUCTR2010-023457-11-BE进行中(未招募)1 期

Immune regulation and timing of chemotherapy in advanced/recurrent ovarian and endometrial cancer - TIREG

Z Leuven0 个研究点目标入组 37 人开始时间: 2011年1月24日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
37

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • -Failure of two lines of cytotoxic chemotherapy (ovarian cancer) or one line of cytotoxic chemotherapy (endometrial cancer)
  • -ECOG Status 1-2
  • -No previous chemotherapy for 3 months
  • -Confirmed histological evidence of either ovarian or primary peritoneal malignancy or endometrial cancer. All histological types will be included.
  • -Assessable disease by imaging (either CT Scan or MRI scan) will need to be present or alternatively, if absent, CA 125 levels should be at least twice normal and shown to have been increased on two occasions at least one week apart.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Documented autoimmune disease
  • -Currently ongoing systemic corticosteroid therapy and/or immune suppressant therapy
  • -Venous access is predicted to obviate frequent blood samples

研究者

发起方
Z Leuven

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