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临床试验/ACTRN12608000170325
ACTRN12608000170325已完成2 期

A Phase II Study to Assess the Effect of Intermittent Androgen Blockade in the Treatment of Advanced Prostate Cancer

Abbott pharmaceuticals Pty Ltd0 个研究点目标入组 250 人开始时间: 2008年4月8日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
ot stated 至 o limit(—)
性别
Male

入选标准

  • Prostate cancer requiring commencement of androgen suppression, and likely to be a candidate for an intermittant program.

排除标准

  • Prior treatment with hormonal therapy, chemotherapy or biologic response modifiers (other than neoadjuvant hormonal therapy that meets the criteria of 3.1.(i)
  • b) Patients presenting with acute or impending cord compression.
  • c) Patients with extensive involvement manifest by a report of ‘superscan’ type uptake pattern.
  • d) History of prior malignancy except for adequately treated basal cell (or squamous cell) skin cancer, or other cancer for which the patient has been disease-free for at least 5 years.
  • e) Patients with known history of hypersensitivity reaction to either study medication or drugs with a similar structure.

研究者

发起方
Abbott pharmaceuticals Pty Ltd

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