NL-OMON46049已完成4 期
A non-interventional biomarker study in patients with NSCLC of adenocarcinoma tumour histology eligible for treatment with Vargatef according to the approved label - Biomarker study in patients with NSCLC
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 34
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Women and men with locally advanced, metastatic or locally recurrent NSCLC with histology of adenocarcinoma
- •- Vargatef is initiated and administered in accordance with the SPC
- •- Available fixed and paraffin embedded (FPE) tumour tissue routinely obtained at diagnosis and/or re-biopsy before the initiation of the first line treatment (either block or slides, minimum of 10 slides and up to 20 slides if possible at 5 um thickness).
排除标准
- •- Any contraindication to Vargatef or docetaxel as specified in their respective labels
- •- Vargatef initiated from more than 7 days prior to inclusion in this NIS
- •- Patients participating simultaneously in another NIS or a clinical trial
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