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临床试验/NCT00770471
NCT00770471已完成1 期

A Phase I/II Trial of Temozolomide and ABT-888 in Subjects With Newly Diagnosed Glioblastoma Multiforme

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins11 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2009年7月13日最近更新:
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
24
试验地点
11
主要终点
Overall survival (Phase II)

研究概览

简要总结

RATIONALE: ABT-888 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving ABT-888 together with radiation therapy and temozolomide may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of ABT-888 when given together with radiation therapy and temozolomide and to see how well it works in treating patients with newly diagnosed glioblastoma multiforme.

详细描述

OBJECTIVES:

Primary

  • To determine the maximum tolerated dose (MTD) of ABT-888 when administered in combination with radiotherapy and temozolomide in patients with newly diagnosed glioblastoma multiforme. (Phase I)
  • To estimate the overall survival of patients treated with ABT-888 when administered at the MTD in combination with radiotherapy and temozolomide. (Phase II)

Secondary

  • To assess the toxicity associated with this regimen. (Phase I)
  • To assess and describe the pharmacokinetics of ABT-888. (Phase I)
  • To estimate the frequency of toxicity associated with this regimen. (Phase II)

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
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

研究组 & 干预措施

Dose Escalation

Experimental

干预措施: gene expression analysis (Genetic)

Dose Escalation

Experimental

干预措施: temozolomide (Drug)

Dose Escalation

Experimental

干预措施: veliparib (Drug)

Dose Escalation

Experimental

干预措施: DNA methylation analysis (Genetic)

Dose Escalation

Experimental

干预措施: mutation analysis (Genetic)

Dose Escalation

Experimental

干预措施: proteomic profiling (Genetic)

Dose Escalation

Experimental

干预措施: high performance liquid chromatography (Other)

Dose Escalation

Experimental

干预措施: immunoenzyme technique (Other)

Dose Escalation

Experimental

干预措施: laboratory biomarker analysis (Other)

Dose Escalation

Experimental

干预措施: mass spectrometry (Other)

Dose Escalation

Experimental

干预措施: pharmacogenomic studies (Other)

Dose Escalation

Experimental

干预措施: pharmacological study (Other)

Dose Escalation

Experimental

干预措施: adjuvant therapy (Procedure)

Dose Escalation

Experimental

干预措施: radiation therapy (Radiation)

结局指标

主要结局

Overall survival (Phase II)

时间窗: continous

Maximum tolerated dose of ABT-888 (Phase I)

时间窗: continous

次要结局

  • Frequency of toxicity (Phase II)(continous)
  • Toxicity (Phase I)(continous)
  • Pharmacokinetics of ABT-888 (Phase I)(continous)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (11)

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