跳至主要内容
临床试验/NCT00356980
NCT00356980已完成1 期

A Phase I Trial of TNF-Bound Colloidal Gold (CYT-6091) by Intravenous Administration in Subjects With Advanced Solid Organ Malignancies

National Institutes of Health Clinical Center (CC)4 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2006年5月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
60
试验地点
4
主要终点
Maximum tolerated dose of TNF-bound colloidal gold (CYT-6091)

研究概览

简要总结

RATIONALE: Biological therapies, such as TNF-bound colloidal gold, may stimulate the immune system in different ways and stop tumor cells from growing.

PURPOSE: This phase I trial is studying the side effects and best dose of TNF-bound colloidal gold in treating patients with advanced solid tumors.

详细描述

OBJECTIVES:

Primary

  • Determine the maximum tolerated dose of TNF-bound colloidal gold (CYT-6091) in patients with advanced solid tumors.
  • Determine the toxicities of CYT-6091 in these patients.

Secondary

  • Determine the pharmacokinetics of CYT-6091 in these patients.
  • Evaluate biopsy samples of tumor and adjoining normal tissue for levels of CYT-6091.
  • Determine if antitumor effects of CYT-6091 occur in these patients.

研究设计

研究类型
Interventional
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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Maximum tolerated dose of TNF-bound colloidal gold (CYT-6091)

Toxicity

次要结局

  • Measurements of CYT-6091 in tumor biopsies
  • Pharmacokinetic profile of CYT-6091
  • Tumor biopsy histology and gene expression after treatment
  • Immunogenicity of CYT-6091
  • Electron microscopy of biopsy to determine presence of colloidal gold
  • Response of target and nontarget lesions
  • Overall response
  • Duration of response
  • Duration of stable disease

研究者

研究点 (4)

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