跳至主要内容
临床试验/CTIS2022-501360-18-00
CTIS2022-501360-18-00招募中1 期

Randomized, Open-Label, Phase 3 Trial of Nivolumab plus Ipilimumab or Nivolumab plus Platinum-Doublet Chemotherapy versus Platinum-DoubletChemotherapy in Early Stage NSCLC - CA209-816

Bristol-Myers Squibb International Corporation0 个研究点目标入组 386 人开始时间: 2023年2月15日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
386

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
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.

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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