跳至主要内容
临床试验/NCT01585974
NCT01585974已完成不适用

Duration of Treatment With TKIs in the Treatment of Metastatic Renal Cell Carcinoma

Bayer0 个研究点目标入组 151 人开始时间: 2012年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Bayer
入组人数
151
主要终点
Duration of treatment: from start of tyrosine kinase inhibitor treatment to permanent discontinuation of the product

研究概览

简要总结

This study is a prospective, non-interventional, non-controlled, multi-center, observational cohort study. The medication is prescribed within the regular practice of the physician. Duration and dosage of treatment is solely at the discretion of the attending physician. The primary objective of this study is to assess duration of treatment in Turkish renal cell carcinoma patients treated with TKIs (Tyrosine Kinase Inhibitors) who could not tolerate prior cytokine treatment within the first month of treatment.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • To be diagnosed as metastatic renal cell carcinoma
  • Previous cytokine therapy
  • To sign informed consent form (ICF)

排除标准

  • Patients not willing to sign informed consent form or who withdraw their consent

结局指标

主要结局

Duration of treatment: from start of tyrosine kinase inhibitor treatment to permanent discontinuation of the product

时间窗: After 2 years

次要结局

  • Incidence of treatment-emergent adverse events (TEAE)(After 2 years)
  • Change of Tumor status(Baseline and 2 years)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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