跳至主要内容
临床试验/NCT02475382
NCT02475382No Longer Available不适用

Expanded Access Program With Nivolumab Monotherapy in Subjects With Advanced or Metastatic Squamous (Sq) or Non-Squamous (Non-Sq) Non-Small Cell Lung Cancer (NSCLC) Who Have Received at Least One Prior Systemic Regimens for the Treatment of Stage IIIb/IV SqNSCLC

Bristol-Myers Squibb2 个研究点 分布在 1 个国家开始时间: 2015年6月18日最近更新:
适应症

试验速览

阶段
不适用
状态
No Longer Available
发起方
试验地点
2

研究概览

简要总结

The purpose of this study is to provide treatment with nivolumab, a fully human monoclonal antibody, to subjects who have relapsed after treatment with a minimum of 1 prior systemic treatment for advanced or metastatic squamous (Sq) or non-squamous (non-Sq) non-small cell lung cancer (NSCLC) , Stage IIIB/IV and whose physicians believe that nivolumab treatment is appropriate.

研究设计

研究类型
Expanded Access

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Sq or Non-Sq NSCLC, Stage IIIb/IV (histologically or cytologically confirmed)
  • Relapsed after 1 prior platinum-based systemic treatment
  • Eastern Cooperative Oncology Group (ECOG) Performance Status < 2
  • CNS metastasis must be treated and returned to baseline at least 2 weeks before first dose of nivolumab and off steroids or using stable or decreasing dose of < 10 mg prednisone or equivalent
  • Prior chemotherapy, Tyrosine Kinase Inhibitor (TKI) therapy or Immunotherapy (tumor vaccine, cytokine or growth factor to control cancer) must be completed at least 2 weeks before first nivolumab dose

排除标准

  • CNS metastases (untreated and/or symptomatic)
  • Carcinomatous meningitis
  • ECOG Performance status > 3
  • Corticosteroids > 10 mg prednisolone/day (or equivalent)
  • Prior treatment with anti-PD-1, anti-PD-L-1, anti-PDL2, anti-CT137 or anti-CTLA antibody, including ipilimumab or any other drugs specifically targeting T cell costimulation or checkpoint pathways

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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