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临床试验/EUCTR2015-000735-32-PL
EUCTR2015-000735-32-PL进行中(未招募)1 期

A Phase 3 Randomized, Placebo-controlled, Double-blind Study of Apalutamide Plus Androgen Deprivation Therapy (ADT) Versus ADT in Subjects with Metastatic Hormone-sensitive Prostate Cancer (mHSPC)

Janssen-Cilag International NV0 个研究点目标入组 1,000 人开始时间: 2015年10月27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
1,000

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

  • - Diagnosis of prostate adenocarcinoma as confirmed by the investigator
  • - Metastatic disease documented by greater than or equal to (>=) 1
  • bone lesions on 99mTc bone scan. Participants with a single bone lesion must have confirmation of bone metastasis by computed tomography (CT) or magnetic resonance imaging (MRI)
  • - Eastern Cooperative Oncology Group Performance Status (ECOG PS) grade of 0 or 1
  • - Participants who received docetaxel treatment must meet the following criteria:
  • a) Received a maximum of 6 cycles of docetaxel therapy for mHSPC;
  • b) Received the last dose of docetaxel <=2 months prior to
  • randomization;
  • c) Maintained a response to docetaxel of stable disease or better, by investigator assessment of imaging and PSA, prior to randomization
  • - Other allowed prior treatment for mHSPC:
  • a) Maximum of 1 course of radiation or surgical intervention; radiation therapy for metastatic lesions must be completed prior to
  • randomization;
  • b) Less than or equal to (<=) 6 months of ADT prior to randomization
  • - Allowed prior treatments for localized prostate cancer (all treatments must have been completed >= 1 year prior to randomization)
  • a) <= 3 years total of ADT;
  • b) All other forms of prior therapies including radiation therapy,
  • prostatectomy, lymph node dissection and systemic therapies
  • 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 600
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 400

排除标准

  • - Pathological finding consistent with small cell, ductal or neuroendocrine carcinoma of the prostate
  • - Known brain metastases
  • - Lymph nodes as only sites of metastases
  • - Visceral (ie, liver or lung) metastases as only sites of metastases
  • - Other prior malignancy less than or equal to 5 years prior to
  • randomization with the exception of squamous or basal cell skin
  • carcinoma or noninvasive superficial bladder cancer
  • - Prior treatment with other next generation anti-androgens or other CYP17 inhibitors, immunotherapy or radiopharmaceutical agents for prostate cancer
  • - History of seizures or medications known to lower seizure threshold

研究者

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