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临床试验/JPRN-jRCT2080221877
JPRN-jRCT2080221877未知1 期

A Study in Japan and Ex-Japan to Characterize the Pharmacokinetic and Pharmacodynamic Response to Orteronel (TAK-700) in Chemotherapy-Naive Patients With Castration-Resistant Prostate Cancer

Takeda Pharmaceutical Company Limited0 个研究点目标入组 72 人开始时间: 2012年8月7日最近更新:
适应症

试验速览

阶段
1 期
入组人数
72

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
Male

入选标准

  • Histologically or cytologically confirmed diagnosis of prostate adenocarcinoma
  • - Progressive disease
  • - Prior surgical castration or concurrent use of an agent for medical castration
  • - Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

排除标准

  • - Received prior chemotherapy for prostate cancer
  • - Documented central nervous system metastases
  • - Current spinal cord compression, bilateral hydronephrosis or current bladder neck outlet obstruction
  • - Uncontrolled cardiovascular condition as specified in study protocol
  • - Uncontrolled nausea, vomiting or diarrhea

研究者

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A Study in Japan and Ex-Japan to Characterize the... | 临床试验