跳至主要内容
临床试验/JPRN-jRCT2080222323
JPRN-jRCT2080222323未知3 期

A RANDOMIZED, PHASE III, MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY AND SAFETY OF ONARTUZUMAB IN COMBINATION WITH ERLOTINIB AS FIRST-LINE TREATMENT FOR PATIENTS WITH MET-POSITIVE UNRESECTABLE STAGE IIIB OR IV NON-SMALL CELL LUNG CANCER (NSCLC) CARRYING AN ACTIVATING EGFR MUTATIO

Chugai Pharmaceutical Co., Ltd.0 个研究点目标入组 300 人开始时间: 2013年12月10日最近更新:
适应症

试验速览

阶段
3 期
入组人数
300

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Adult patients, >/= 18 years of age
  • - Histologically confirmed, unresectable Stage IIIB or IV non-small cell lung cancer (NSCLC)
  • - No prior treatment for unresectable Stage IIIB or IV NSCLC
  • - Measurable radiographic evidence of disease according to RECIST v1.1
  • - ECOG performance status of 0 or 1

排除标准

  • - Prior exposure to agents targeting either the HGF or MET pathway
  • - Exposure to an investigational or marketed agent that can act by EGFR inhibition
  • - Pleural effusion, pericardial fluid, or ascites requiring drainage every other week or more frequently
  • - Brain metastasis or spinal cord compression not definitively treated with surgery and/or radiation, or previously diagnosed and treated central nervous system (CNS) metastases or spinal cord compression without evidence of clinically stable disease for >/= 14 days
  • - History of another malignancy in the previous 5 years, unless cured by surgery alone and continuously disease-free
  • - Radiographically evident interstitial lung disease , concurrent infection, or a history of any of these conditions
  • - Inadequate hematologic, biochemical, and organ function
  • - Pregnant or lactating women
  • - Life expectancy of < 12 weeks
  • - Receipt of an investigational drug within 28 days prior to initiation of study treatment

研究者

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