跳至主要内容
临床试验/EUCTR2008-000213-30-DE
EUCTR2008-000213-30-DE进行中(未招募)不适用

Extension study to evaluate long-term-safety of IMA901 plus GM-CSF in advanced renal cell carcinoma patients who achieved a decrease in tumor load or stabilization of their disease after participation in the open-label, multicenter IMA901-202 Phase 2 study

immatics biotechnologies GmbH0 个研究点目标入组 20 人开始时间: 2008年2月25日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
20

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

  • 1. Patients who have participated in the core study IMA901-202 over the entire scheduled period and were compliant with the protocol
  • 2. Patients who achieved a decrease in tumor load or stabilization of their disease after participation in the core study IMA901-202
  • 3. Ability to understand the nature of the study and to give written informed consent
  • 4. Willingness and ability to comply with the study protocol for the duration of the study
  • 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

  • 1. Non compliance in the conduct of the IMA901-202 study
  • 2. Women or men who decline to practice a medically approved method of contraception
  • 3. Pregnancy or breastfeeding
  • 4. Any condition which in the judgement of the investigator would place the patient at undue risk

研究者

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