EUCTR2016-003536-21-GR进行中（未招募）1 期
Randomized, Open-Label, Phase 3 Trial of Nivolumab plus Ipilimumab or Nivolumab plus Platinum-Doublet Chemotherapy versus Platinum-Doublet Chemotherapy in Early Stage NSCLC - CheckMate 816: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 816
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 350
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
- •Early stage (IB - IIIA), operable non-small cell lung cancer, confirmed in tissue.
- •Lung function capacity capable of tolerating the proposed lung surgery
- •Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1
- •Available tissue of primary lung tumor.
- •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 140
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 210
排除标准
- •Presence of locally advanced, inoperable or metastatic disease.
- •Participants with active, known or suspected autoimmune disease.
- •Prior treatment with any drug that targets T cell co-stimulations pathways (such as checkpoint inhibitors).
研究者
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