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临床试验/NCT00022425
NCT00022425Unknown1 期

Multiple-Dose Phase I and Pharmacokinetic Trial of Perillyl Alcohol

The Cleveland Clinic2 个研究点 分布在 1 个国家开始时间: 2001年6月最近更新:
适应症
相关药物

试验速览

阶段
1 期
试验地点
2

研究概览

简要总结

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the recurrence of cancer. The use of perillyl alcohol may be effective in preventing the recurrence of breast cancer.

PURPOSE: Phase I trial to study the effectiveness of perillyl alcohol in preventing the recurrence of breast cancer in women who have been treated with surgery with or without adjuvant therapy.

详细描述

OBJECTIVES:

  • Determine the maximum tolerated dose of perillyl alcohol in women at risk for recurrent breast cancer.
  • Determine the toxicity of this drug in these patients.
  • Determine the single-dose and multiple-dose pharmacokinetics of this drug in these patients.

OUTLINE: This is a dose-escalation study.

Patients receive oral perillyl alcohol once daily on days 1-28. Treatment continues every 4 weeks for 3 courses.

Cohorts of 6 patients receive escalating doses of perillyl alcohol until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience grade 1 toxicity or at least 1 of 6 patients experience grade 2 or greater toxicity.

研究设计

研究类型
Interventional
主要目的
Prevention

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究者

申办方类型
Other

研究点 (2)

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