EUCTR2012-004707-12-NL进行中（未招募）1 期
An open-label, multi-center everolimus roll-over protocol for patients who have completed a previous Novartis-sponsored everolimus study and are judged by the investigator to benefit from continued everolimus treatment
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 13
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.Patient is currently enrolled in a Novartis-sponsored, CD&MA study receiving everolimus or everolimus plus Sandostatin LAR® Depot and has fulfilled all their requirements in the parent study.
- •2.Patient is currently benefiting from the treatment with everolimus, as determined by the guidelines of the parent protocol.
- •Other protocol defined inclusion criteria may apply
- •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 12
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 6
排除标准
- •1.Patient has been permanently discontinued from everolimus study treatment in the parent study.
- •2.Patient is receiving everolimus in combination with unapproved or experimental treatments.
- •Other protocol defined exclusion criteria may apply
研究者
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