跳至主要内容
临床试验/NCT00293371
NCT00293371终止1 期

A Phase I/II Study of Docetaxel/Prednisone and PTK 787/ZK 222584 in Previously Untreated Metastatic Hormone Refractory Prostate Cancer

University of California, San Francisco2 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2005年2月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
终止
入组人数
6
试验地点
2
主要终点
Time to prostate-specific antigen (PSA) and objective progression

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. Vatalanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving vatalanib together with docetaxel and prednisone may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of vatalanib when given together with docetaxel and prednisone and to see how well they work in treating patients with advanced prostate cancer.

详细描述

OBJECTIVES:

Primary

  • Determine the dose-limiting toxicities and maximum tolerated dose of vatalanib when used in combination with docetaxel and prednisone in patients with chemotherapy-naive, metastatic, hormone-refractory prostate cancer. (phase I)

Secondary

  • Determine alterations in pharmacokinetics of docetaxel and vatalanib in these patients. (phase I)
  • Determine the clinical efficacy of this regimen as measured by declines in prostate-specific antigen, measurable disease response, time to progression, and overall survival. (phase II)

研究设计

研究类型
Interventional
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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Time to prostate-specific antigen (PSA) and objective progression

Response rate (PSA and objective)

Toxicity

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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