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临床试验/NCT01132014
NCT01132014已完成早期 1 期

A Pilot Clinical Trial of Dendritic Cell Vaccine Loaded With Autologous Tumor for Recurrent Ovarian, Primary Peritoneal or Fallopian Tube Cancer

Abramson Cancer Center at Penn Medicine2 个研究点 分布在 1 个国家目标入组 67 人开始时间: 2010年5月最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
67
试验地点
2
主要终点
Safety

研究概览

简要总结

This is a Five cohort sequential clinical trial for subjects with recurrent ovarian, fallopian tube, or primary peritoneal cancer to determine the feasibility and safety as well as immunogenicity of OC-DC, an autologous vaccine comprised of autologous dendritic cells (DC) loaded in vitro with lysate from autologous oxidized tumor cells, administered intranodally alone, or in combination with intravenous Bevacizumab and cyclophosphamide or in combination with intravenous Bevacizumab, cyclophosphamide and aspirin. Study duration is 24 months.

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 —(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

时间窗: 30 days of last vaccination

Safety will be established by grading the observed toxicities using the NCI Common Toxicity Criteria (CTC Version3.0). All toxicities observed within 30 days of last vaccination will be included.

次要结局

  • Dose limiting toxicity
  • Clinical Response
  • Immune Response Immune Response

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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Autologous OC-DC Vaccine in Ovarian Cancer | 临床试验