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临床试验/EUCTR2004-000808-40-LT
EUCTR2004-000808-40-LT进行中(未招募)不适用

Randomized, open label, multi-center, phase III study onpharmacokinetics, pharmacodynamics, efficacy and safety ofGoserelin 1M Implant HEXAL in patients with advancedprostatic cancer in comparison to Zoladex® 3.6 mg - Gosezol

Hexal AG0 个研究点目标入组 90 人开始时间: 2004年11月10日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Hexal AG
入组人数
90

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

  • Histologically confirmed diagnosis of advanced adenocarcinoma of the prostate
  • stage T3-4N0M0, T1-4N1M0 or T1-4N0-1M1,
  • either as newly (within the past 4 weeks) diagnosed adenocarcinoma of the
  • or recurrence of adenocarcinoma of the prostate after previous
  • prostatectomy and/or radiotherapy and/or brachytherapy
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1) Patients expected to require additional anti-neoplastic treatment during the study
  • 2) Patients at particular risk of developing urethral obstructions and/or spinal cord
  • compression

研究者

发起方
Hexal AG

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