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临床试验/EUCTR2017-001626-17-DE
EUCTR2017-001626-17-DE进行中(未招募)1 期

A Phase 2 Study of Nivolumab in Combination with Either Rucaparib, Docetaxel, or Enzalutamide in Men with Castration-resistant Metastatic Prostate Cancer - CheckMate 9KD: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 9KD

Bristol-Myers Squibb International Corporation0 个研究点目标入组 330 人开始时间: 2017年11月15日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
330

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
Male

入选标准

  • - Histologic confirmation of adenocarcinoma of the prostate
  • - Evidence of stage IV disease
  • - Ongoing androgen deprivation therapy (ADT) with a gonadotropin-releasing hormone (GnRH) analogue or bilateral orchiectomy
  • - Mandatory plasma and, fresh or archival tumor tissue must be submitted
  • 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 150
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 150

排除标准

  • - Prior malignancy active within the previous 3 years except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the breast
  • - Participants with active brain metastases
  • - Participants must have recovered from the effects of major surgery requiring general anesthesia or significant traumatic injury at least 14 days before treatment arm assignment

研究者

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