跳至主要内容
临床试验/JPRN-UMIN000023763
JPRN-UMIN000023763招募中2 期

The Phase II study on the efficacy and safety of weekly nab-paclitaxel with 3 rd line therapy or more of advanced or recurrent non-small cell lung cancer after disease progression on 2nd line therapy or more - The Phase II study on the efficacy and safety of weekly nab-paclitaxel with 3 rd line therapy or more of advanced or recurrent non-small cell lung cancer after disease progression on 2nd line therapy or more

Division of Medical Oncology Department of Internal Medicine Teikyo University School of Medicine0 个研究点目标入组 36 人开始时间: 2016年8月25日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
36

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Patients with paclitaxel treatment history. 2.Patients with hypersensitivity to paclitaxel or preparations containing albumin. 3.Patients with active double cancer in need of treatment. However it is not excluded that carcinoma in situ that is judged to be healing by local treatment, intramucosal cancer equivalent of lesions or other cancers unlikely in need of treatment. 4.The infection requiring systemic treatment (including patient of HBs antigen-positive). 5.Serious complications (heart disease, interstitial pneumonia, uncontrolled high blood pressure or diabetes, etc.) 6.there is a possibility of pregnancy or during pregnancy or lactating women. 7.Patients with psychosis or psychotic symptoms is determined to be difficult to participants in a clinical trial. 8.Patients during systemic administration steroids therapy(oral or intravenous). 9.Patients with symptomatic brain metastases. 10.Other, cases physicians it is judged unsuitable for registration of this clinical trial.

研究者

发起方
Division of Medical Oncology Department of Internal Medicine Teikyo University School of Medicine

相似试验

The Phase II study on the efficacy and safety of... | 临床试验