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临床试验/EUCTR2006-006626-26-IT
EUCTR2006-006626-26-IT进行中(未招募)不适用

A phase III, multicenter, placebo-controlled, double-blind, randomized clinical trial to evaluate the efficacy of bevacizumab in combination with Tarceva (erlotinib) compared with Tarceva alone for treatment of advanced Non Small Cell Lung Cancer (NSCLC) after failure of standard first-Line chemotherapy - ND

GENENTECH , INC0 个研究点目标入组 650 人开始时间: 2007年7月13日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
650

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

  • Patients must fulfill all of the following criteria to be eligible for study entry: Signed written informed consent Cytologically or histologically confirmed NSCLC Clinical or radiographic progression during or after first-line chemotherapy or chemoradiotherapy for NSCLC Consent to provide archival tissue for analysis is required for participation in this study. Patients who consent to provide tissue but whose archival tissue is found to be inadequate (e.g., stained slides) remain eligible for study participation ECOG performance status of 0, 1, or 2 (see Appendix F) Age >= 18 years
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients meeting any of the following criteria will be ineligible for study entry: Squamous cell carcinoma, except for patients with no intrathoracic disease or small peripheral lesions only Prior treatment with an investigational or marketed inhibitor of the EGFR pathway or anti-angiogenesis agent Systemic chemotherapy, radiotherapy, or investigational treatment within 28 days prior to randomization

研究者

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