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临床试验/EUCTR2008-008478-30-DE
EUCTR2008-008478-30-DE进行中(未招募)不适用

[Targetspezifische Second-line-Therapie des metastasierten Urothelkarzinoms mit Temsirolimus]Target-specific therapy of metastatic urothelial carcinoma with temsirolimus - Targetspezifische Second-line-Therapie des metastasierten Urothelkarzinoms mit Temsirolimus

ukaskrankenhaus GmbH0 个研究点开始时间: 2009年1月20日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • men and women,
  • at least 18 years
  • metastatic urothelial carcinoma
  • prvious chemotherapy with a cis-platin containing regimen
  • life expectancy
  • at least 6 months
  • karnofsky index at least 60%
  • 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

  • Impaired general health status, defined as Karnofsky-Index < 60%
  • Previous treatment with temsirolimus
  • Cardiac failure of NYHA stage 3 or 4
  • Psychiatric disorder
  • Pregnancy, lactation
  • Second malignant disease (exception: basalioma of skin) in previous 2 years
  • Participation in another therapeutical trial during 60 days preceding study start
  • Contraindications according to SmPC: Hypersensitivity to temsirolimus, its metabolites (including sirolimus), polysorbate 80, or to any of the excipients of temsirolimus

研究者

发起方
ukaskrankenhaus GmbH

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