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临床试验/EUCTR2007-007460-22-SE
EUCTR2007-007460-22-SE进行中(未招募)不适用

International Survival Follow-up of Patients Enrolled In the Renal Cell Carcinoma Evaluation of Adjuvant Oncophage® Treatment in the Antigenics C-100-12 (Part I) Protocol (INSPIRE). - INSPIRE

Antigenics Inc.0 个研究点目标入组 436 人开始时间: 2008年2月12日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
436

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • To be eligible, patients must have:
  • 1.Participated in the Antigenics C-100-12 (Part I) protocol and terminated the study with the last survival status reported as alive” and due to administrative study closure”.
  • 2.Signed an informed consent to participate in the C-100-27 Survival Follow-up protocol, and be willing to receive contact from a representative from the protocol investigative study centers and/or any subsequently identified co-investigator sites where patients consent to continued survival follow-up and/or a member from a company designated by the Sponsor every 6 months if no disease recurrence and every 3 months if disease has recurred.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • The study has no exclusion criteria.

研究者

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