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临床试验/NCT00003712
NCT00003712已完成1 期

A Phase I Study of the Safety, Tolerability, and Pharmacokinetics of Intravenous CCI-779 Given Once Daily for 5 Days Every 2 Weeks to Patients With Advanced Solid Tumors

The University of Texas Health Science Center at San Antonio2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2001年1月1日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
15
试验地点
2

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

PURPOSE: Phase I trial to study the effectiveness of CCI-779 in treating patients who have advanced solid tumors.

详细描述

OBJECTIVES:

  • Determine the safety, tolerability, and maximum tolerated dose (MTD) of CCI-779 in patients with advanced solid tumors (part I) who are not receiving anticonvulsant therapy.
  • Determine the safety, tolerability, and MTD in patients with recurrent gliomas or brain metastases (part II) who are receiving anticonvulsant therapy.
  • Determine the preliminary pharmacokinetic profile and antitumor activity of CCI-779 in these patients.

OUTLINE: This is an open-label, dose-escalation study.

  • Part I: Patients receive CCI-779 IV over 30 minutes on days 1-5, followed by a 9 day rest period. Treatment courses repeat every 2 weeks in the absence of disease progression or unacceptable toxicity.

The maximum tolerated dose for part I is defined as the dose level at which 33% of patients experience dose limiting toxicity.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •DISEASE CHARACTERISTICS:
  • •Histologically proven advanced solid tumors that are refractory or for which no curative therapy exists
  • •No CNS metastases, peritumoral edema, or symptomatic brain metastases (part I)
  • •Measurable or evaluable disease
  • •Histologically proven recurrent gliomas or brain metastases for which no curative therapy exists
  • •Receiving anticonvulsants
  • •Measurable or evaluable disease
  • •PATIENT CHARACTERISTICS:
  • •18 and over
  • •Performance status:
  • •Life expectancy:
  • •At least 3 months
  • •Hematopoietic:
  • •Absolute neutrophil count at least 1,500/mm^3
  • •Platelet count at least 100,000/mm^3
  • •Hemoglobin at least 9 g/dL
  • •Bilirubin less than 1.5 mg/dL
  • •AST or ALT less than 3 times upper limit of normal (ULN) (less than 5 times ULN if liver metastases)
  • •Creatinine less than 2 mg/dL
  • •Cardiovascular:
  • •No unstable angina
  • •No myocardial infarction within past 6 months
  • •No maintenance therapy for life-threatening arrhythmias
  • •Not pregnant or nursing
  • •Fertile patients must use effective contraception
  • •HIV negative
  • •No active infection or other serious concurrent illness
  • •Triglycerides no greater than 300 mg/dL
  • •Cholesterol no greater than 350 mg/dL
  • •No known hypersensitivity to macrolide antibiotics (e.g., clarithromycin, erythromycin, or azithromycin)
  • •PRIOR CONCURRENT THERAPY:
  • •Biologic therapy:
  • •Not specified
  • •Chemotherapy:
  • •At least 3 weeks since prior chemotherapy (6 weeks since nitrosoureas and mitomycin)
  • •No other concurrent chemotherapy
  • •Endocrine therapy:
  • •Concurrent corticosteroids used to reduce edema in patients with primary or metastatic CNS tumors allowed
  • •No concurrent hormonal therapy
  • •Radiotherapy:
  • •At least 3 weeks since prior radiotherapy
  • •No concurrent radiotherapy
  • •Not specified
  • •At least 1 month since prior investigational agents
  • •At least 3 weeks since prior immunosuppressive therapy
  • •No concurrent anticonvulsant therapy (part I)
  • •No concurrent immunosuppressive therapy (e.g., terfenadine, cisapride, astemizole, pimozide)
  • •No known agents that inhibit or induce cytochrome p450

排除标准

  • 未提供

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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