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临床试验/EUCTR2015-000735-32-RO
EUCTR2015-000735-32-RO进行中(未招募)不适用

A Phase 3 Randomized, Placebo-controlled, Double-blind Study of JNJ-56021927 Plus Androgen Deprivation Therapy (ADT) Versus ADT in Subjects with Low-volume 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: 2016年2月16日最近更新:
适应症

试验速览

阶段
不适用
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

  • - Adenocarcinoma of prostate; if diagnosed greater than or equal to (>=) 5 years from randomization, histologic evidence of prostate adenocarcinoma from a metastatic lesion is required
  • - Metastatic disease documented by >= 2 bone lesions on 99mTc bone scan
  • - Eastern Cooperative Oncology Group Performance Status (ECOG PS) grade of 0, 1, or 2
  • - Allowed prior treatment for prostate cancer:
  • a) Maximum of 1 course of radiation or surgical intervention;
  • b) Up to 6 cycles of docetaxel for low-volume disease with the last dose within 2 months of randomization;
  • c) Must not have experienced disease progression between the last dose of docetaxel and Screening;
  • d) Participants who did not receive prior docetaxel may have received less than or equal to (<=) 3 months of ADT in the metastatic disease setting prior to randomization. Participants who received prior docetaxel may have received <= 6 months ADT in the metastatic setting prior to randomization;
  • e) May also have received up to 6 months of GnRHa in the adjuvant or neo-adjuvant setting as long as it was completed greater than (>)1 year prior to randomization; f) May have received radiation therapy or prostatectomy as definitive therapy
  • 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 site of metastasis
  • - Visceral metastasis observed on computed tomography (CT)/magnetic resonance imaging (MRI) or >= 4 bone lesions on 99mTc bone scan with at least 1 lesion beyond the pelvis or vertebral column
  • - Any prior malignancy within 5 years prior to randomization with the exception of squamous or basal cell skin carcinoma or non-invasive superficial bladder cancer
  • - Prior treatment with other second 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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