跳至主要内容
临床试验/NCT00101257
NCT00101257已完成1 期

Phase I Study to Evaluate the Safety of Cellular Adoptive Immunotherapy Using Autologous CD4+ Antigen-Specific T Cell Clones for Patients With Advanced Ovarian Cancer

Fred Hutchinson Cancer Center2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2004年10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
18
试验地点
2
主要终点
Safety and toxicity

研究概览

简要总结

RATIONALE: Biological therapies, such as cellular adoptive immunotherapy, 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 cellular adoptive immunotherapy in treating patients with stage III or stage IV ovarian cancer or primary peritoneal cancer.

详细描述

OBJECTIVES:

Primary

  • Determine the safety and toxicity of autologous CD4-positive antigen-specific T cells in patients with stage III or IV ovarian epithelial cancer or primary peritoneal cavity cancer.
  • Determine the duration of in vivo persistence of this drug in these patients.

Secondary

  • Determine the antitumor effect of this drug in these patients.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

年龄范围
18 Years 至 75 Years(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

结局指标

主要结局

Safety and toxicity

Duration of in vivo persistence

Antitumor effects

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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