跳至主要内容
临床试验/NCT00667641
NCT00667641已完成1 期

Phase I Study of Paclitaxel (Taxol) and Bortezomib (Velcade) in Patients With Refractory Solid Tumor Malignancies Involving an Activated MAPK Pathway

University of Medicine and Dentistry of New Jersey2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2007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
16
试验地点
2
主要终点
Maximum tolerated dose of paclitaxel in combination with bortezomib

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving paclitaxel together with bortezomib may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of paclitaxel and bortezomib in treating patients with metastatic or unresectable malignant solid tumors.

详细描述

OBJECTIVES:

Primary

  • To identify the maximum tolerated dose of paclitaxel in combination with bortezomib in patients with metastatic or unresectable solid tumor malignancies that involve an activated Ras/Raf/MAPK pathway.

Secondary

  • To assess the toxicity of this regimen.
  • To assess tumor response in these patients.
  • To determine whether Bim is upregulated in peripheral blood mononuclear cells obtained from patients treated with this regimen.
  • To correlate markers of Ras/Raf/MAPK pathway activation in fresh or archived tumor tissue with clinical response in these patients.
  • To perform pharmacokinetic (PK) studies to determine whether bortezomib alters paclitaxel PK parameters.

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
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 of paclitaxel in combination with bortezomib

时间窗: 2 years

次要结局

未报告次要终点

研究者

研究点 (2)

Loading locations...

相似试验