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临床试验/NCT00104130
NCT00104130终止2 期

A Phase 2 Study of KOS-862 Administered Intravenously Weekly for 3 Weeks Every 4 Weeks, in Patients With Hormone Resistant Prostate Cancer Who Have Progressed Following Initial Therapy for Metastatic Disease

Bristol-Myers Squibb18 个研究点 分布在 1 个国家目标入组 53 人开始时间: 2004年12月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
53
试验地点
18
主要终点
prostate cancer

研究概览

简要总结

The purpose of this trial is to study KOS-862 in men with metastatic prostate cancer who have failed a docetaxel-containing regimen.

详细描述

This study is a Phase 2, single arm study of KOS-862 in men with metastatic prostate cancer who have failed a docetaxel-containing regimen. PSA response is the primary end-point and objective responses will be checked as available.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • At least 18 years of age.
  • Metastatic disease.
  • One previous treatment including docetaxel (Taxotere).
  • At least 3 weeks since last surgery/radiation/chemotherapy
  • ECOG Performance Status of 0, 1 or 2

排除标准

  • Active brain metastases

结局指标

主要结局

prostate cancer

prostate-specific antigen (PSA) response

次要结局

未报告次要终点

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry

研究点 (18)

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