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临床试验/NCT00290680
NCT00290680已完成1 期

Phase I Trial of Bortezomib (VELCADE™) and Celecoxib in Patients With Advanced Solid Tumors

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2005年3月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
36
试验地点
2
主要终点
Maximum tolerated dose

研究概览

简要总结

RATIONALE: Bortezomib and celecoxib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving bortezomib together with celecoxib may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of bortezomib and celecoxib in treating patients with advanced solid tumors.

详细描述

OBJECTIVES:

Primary

  • Determine the maximum tolerated dose (MTD) of bortezomib and celecoxib in patients with advanced solid tumors.

Secondary

  • Determine the overall pattern of toxicities associated with this combination, including the emergence of any cumulative toxicities, during multiple courses of this regimen.
  • Describe the response rate and duration of response or disease stability during therapy in the subset of patients with measurable disease.
  • Assess changes in plasma/serum sphingosine-1-phosphate, ceramide, and other markers of the apoptotic pathway before and during therapy.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
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

Maximum tolerated dose

次要结局

  • Response and disease progression by RECIST criteria before each course

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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