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
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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