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临床试验/EUCTR2017-003565-10-DE
EUCTR2017-003565-10-DE进行中(未招募)1 期

eoadjuvant and adjuvant durvalumab in combination with neoadjuvant chemotherapy in patients with operable urothelial cancer. A multicenter, single-arm phase II Trial.

Swiss Group for Clinical Cancer Research0 个研究点目标入组 61 人开始时间: 2018年11月19日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
61

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
All

入选标准

  • - histologically proven urothelial cell carcinoma of the bladder, urethra or upper urinary tract and considered suitable for curative multimodality treatment including surgery by a multidisciplinary tumor board
  • - all histological subtypes eligible if urothelial carcinoma predominant
  • - WHO performance Status 0-1
  • - adequate bone marrow, hepatic, renal and cardiac function
  • 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 37
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 24

排除标准

  • - pathological evidence of small-cell carcinoma component
  • - presence of distant metastasis
  • - previous Treatment with a PD-1 or PD-L1 Inhibitor, including durvalumab
  • - current or prior use of immunosuppressiva medication within 28 days prior to Registration
  • - active or prior documented autoimmune or inflammatory disorders
  • - known history of human immunodeficiency virus (HIV) or active chronic Hepatitis C or Hepatitis B virus infection

研究者

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