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临床试验/JPRN-UMIN000020976
JPRN-UMIN000020976已完成2 期

A study to evaluate the safety of Nivolumab in elderly patients with previously treated non-small cell lung cancer - A study to evaluate the safety of Nivolumab in elderly patients with previously treated non-small cell lung cancer

Hiroshima University Hospital0 个研究点目标入组 30 人开始时间: 2016年2月10日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
30

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
75years-old 至 100years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Subjects with interstitial lung disease which is detected by chest X-ray 3)Subjects with previous malignancies are excluded unless a complete remission was achieved at least 5 years prior to study entry. 4)Uncontrolled intercurrent illness including symptomatic cardiac arrhythmia, or diabetes, Intestinal obstruction. 5)known or suspected autoimmune disease, or receiving continuous systemic corticosteroid or immunosuppressant treatment. 6)Subjects with symptomatic CNS metastases or symptomatic carcinomatous meningitis. Subjects with asymptomatic CNS metastases, and subjects after 4 weeks from whole brain radiation therapy or 2 weeks from stereotactic brain radiation therapy can be included. 7)Radiation therapy within 4 weeks of the first dose of Nivolumab. 8)Subjects with known infection with HIV or AIDS . Positive test for hepatitis B virus antigen or hepatitis C virus indicating acute or chronic infection. 9)Prior therapy with antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways 10)Dementia or psychological disorder difficult to participate in this clinical study.

研究者

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