EUCTR2019-000061-20-PL进行中（未招募）1 期
An open-label, multicenter rollover study to provide continued treatment with anetumab ravtansine for participants with solid tumors who were enrolled in previous Bayer-sponsored studies.
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- Bayer AG
- 入组人数
- 17
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
- •Participants ongoing in an applicable Bayer-sponsored anetumab ravtansine parent study at the time of its planned study closure.
- •For on-treatment participants: participant is eligible to receive the next dose of study intervention per the parent study protocol.
- •For on-treatment participants: any ongoing adverse events that require temporary treatment interruption must be resolved to baseline grade or assessed as stable and not requiring further treatment interruption.
- •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 8
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 9
排除标准
- •For on-treatment participants: a positive serum pregnancy test.
- •For on-treatment participants: use of one or more of the prohibited medications listed in the respective parent study protocol.
- •Participants who are receiving SOC agent(s) but not anetumab ravtansine in the parent study, and are able to receive SOC agent outside of the clinical study.
研究者
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