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临床试验/JPRN-UMIN000021560
JPRN-UMIN000021560已完成未知

A study to evaluate the relation between the efficacy and early Immune Related Advers Events of Nivolmab in patients with non-small cell lung cancer - A study to evaluate the relation between the efficacy and early Immune Related Advers Events of Nivolmab in patients with non-small cell lung cancer

Kobe city medical center general hospital0 个研究点目标入组 43 人开始时间: 2016年3月24日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
43

研究概览

简要总结

Patients with irAEs were associated with a significantly longer median progression-free survival than those without. These findings were comparable to those for patients with and without irAEs 6 weeks after commencement of nivolumab treatment.

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 100years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Subjects with autoimmune disease. 2)Subjects with interstitial lung disease. 3)Receiving continuous systemic corticosteroid. 4)Prior therapy with antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways. 5)Dementia or psychological disorder difficult to participate in this clinical study. 6)Uncontrolled intercurrent illness including symptomatic cardiac arrhythmia, or diabetes, Intestinal obstruction.

研究者

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