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临床试验/EUCTR2014-005614-29-FR
EUCTR2014-005614-29-FR进行中(未招募)不适用

A Phase 2 multicenter, randomized, placebo controlled, double-blind study to assess the safety and efficacy of CC-486 (oral azacitidine) in combination with pembrolizumab (MK-3475) versus pembrolizumab plus placebo in subjects with previously treated locally advanced or metastatic non-small cell lung cancer

Celgene Corporation0 个研究点目标入组 90 人开始时间: 2015年8月6日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
90

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

  • -Subject is = 18 years of age at the time of signing the informed consent form.
  • -Subject has histologically or cytologically confirmed squamous or non-squamous NSCLC.
  • -Subject has stage IIIB or IV NSCLC and was pretreated with 1 prior systemic platinum based chemotherapy.
  • -Subject has provided a formalin fixed tumor tissue sample from a biopsy of a tumor lesion either at the time of or after the diagnosis of metastatic disease has been made AND from a site not previously irradiated to assess for PD-L1 status.
  • -Subject has radiographically-documented measurable disease, as per RECIST 1.1.
  • -Subject has an ECOG performance status of 0 to 1.
  • -Subject has adequate organ and bone marrow functions
  • 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 30
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 60

排除标准

  • -Subject has known sensitizing EGFR and/or positive ALK mutation
  • -Subject has received prior therapy with any other anti-PD-1, or PD-L1 or PD-L2 agent or an antibody targeting other immuno-regulatory receptors or mechanism
  • -Subject has had radiotherapy = 4 weeks or limited field radiation for palliation = 2 weeks prior to starting IP, and/or from whom = 30% of the bone marrow was irradiated.
  • -Subject has received a live-virus vaccination within 30 days of planned treatment start. Seasonal flu vaccines that do not contain live virus are permitted
  • -Subject has active autoimmune disease that has required systemic treatment within the past 2 years
  • -Subject with uncontrolled or symptomatic central nervous system (CNS) metastases and/or carcinomatous meningitis

研究者

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