跳至主要内容
临床试验/NCT00258388
NCT00258388已完成2 期

A Randomized Phase II Study of OGX-011 in Combination With Docetaxel and Prednisone or Docetaxel and Prednisone Alone in Patients With Metastatic Hormone Refractory Prostate Cancer

NCIC Clinical Trials Group13 个研究点 分布在 2 个国家目标入组 82 人开始时间: 2005年9月28日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
82
试验地点
13
主要终点
Prostate-specific antigen (PSA) response measured by Bubley criteria at completion of study

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as docetaxel and prednisone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. OGX-011 may help docetaxel and prednisone kill more tumor cells by making tumor cells less resistant to the drugs.

PURPOSE: This randomized phase II trial is studying how well giving docetaxel and prednisone with or without OGX-011 works in treating patients with recurrent or metastatic prostate cancer that did not respond to previous hormone therapy.

详细描述

OBJECTIVES:

Primary

  • Determine the efficacy, in terms of prostate-specific antigen response, of docetaxel and prednisone with or without OGX-011 in patients with hormone-refractory locally recurrent or metastatic prostate cancer.

Secondary

  • Determine the objective response rate and duration in patients treated with these regimens.
  • Determine the safety and toxic effects of these regimens in these patients.
  • Determine the overall and progression-free survival of patients treated with these regimens.

研究设计

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

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Docetaxel plus prednisone

Active Comparator

干预措施: prednisone (Drug)

OGX011, Docetaxel and Prednisone

Active Comparator

干预措施: custirsen sodium (Drug)

OGX011, Docetaxel and Prednisone

Active Comparator

干预措施: docetaxel (Drug)

OGX011, Docetaxel and Prednisone

Active Comparator

干预措施: prednisone (Drug)

Docetaxel plus prednisone

Active Comparator

干预措施: docetaxel (Drug)

结局指标

主要结局

Prostate-specific antigen (PSA) response measured by Bubley criteria at completion of study

时间窗: 2 years

次要结局

  • Toxicity(2 years)
  • Time to treatment failure(2 years)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (13)

Loading locations...

相似试验