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临床试验/NCT00174434
NCT00174434已完成1 期

A Phase 1 Study Of Paclitaxel In Combination With SU011248 For Patients With Breast Cancer As First-Line Treatment In The Advanced Disease Setting

Pfizer1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2005年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
Pfizer
入组人数
22
试验地点
1
主要终点
Safety of the combination of SU011248 and paclitaxel

研究概览

简要总结

This study is to evaluate the safety of SU011248 in combination with paclitaxel in patients with metastatic or locally recurrent breast cancer who have not received chemotherapy treatment in the advanced disease setting.

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

  • Breast cancer with evidence of unresectable, locally recurrent or metastatic disease.
  • Candidate for treatment with paclitaxel.

排除标准

  • Prior chemotherapy in the advanced disease setting.
  • HER2 positive disease unless previously treated with trastuzumab.

研究组 & 干预措施

A

Experimental

干预措施: SU011248 (Drug)

A

Experimental

干预措施: Paclitaxel (Drug)

结局指标

主要结局

Safety of the combination of SU011248 and paclitaxel

时间窗: 9/05-7/07

次要结局

  • Pharmacokinetics of each medication(9/05-7/07)
  • Objective disease response(9/05-7/07)
  • Progression-free survival.(9/05-7/07)

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (1)

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