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临床试验/NCT00003288
NCT00003288已完成1 期

A Trial of Tirapazamine and Cyclophosphamide in Children With Refractory Solid Tumors

National Cancer Institute (NCI)28 个研究点 分布在 2 个国家目标入组 12 人开始时间: 1998年8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
入组人数
12
试验地点
28

研究概览

简要总结

Phase I trial to study the effectiveness of tirapazamine plus cyclophosphamide in treating children who have refractory solid tumors. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells.

详细描述

OBJECTIVES:

I. Determine the maximum tolerated dose and the dose limiting toxicity of tirapazamine when administered with cyclophosphamide as intravenous infusions to children with refractory solid tumors.

II. Determine the incidence and severity of other toxicities of tirapazamine and cyclophosphamide in these patients.

III. Determine a safe and tolerable dose of tirapazamine administered with cyclophosphamide for a phase II study for the same indications.

IV. Determine the pharmacokinetics of tirapazamine in children and adolescents receiving the combination of tirapazamine and cyclophosphamide.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 21 Years(Child, 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

研究组 & 干预措施

Arm I

Experimental

See arm description.

干预措施: filgrastim (Biological)

Arm I

Experimental

See arm description.

干预措施: cyclophosphamide (Drug)

Arm I

Experimental

See arm description.

干预措施: tirapazamine (Drug)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (28)

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