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临床试验/JPRN-UMIN000015193
JPRN-UMIN000015193
招募中
1 期

Phase I of Vorinostat-Iressa combined therapy on resistance by BIM polymorphysim in EGFR Mutant Lung Cancer - VICTORY-J(Vorinostat-Iressa Combined Therapy on Resistance by BIM Polymorphysim in EGFR Mutant Lung Cancer-JAPAN)

Cancer Research Center, Kanazawa University0 个研究点目标入组 18 人2014年9月17日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
on-small-cell lung cancer
发起方
Cancer Research Center, Kanazawa University
入组人数
18
状态
招募中
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2014年9月17日
结束日期
2016年4月30日
最后更新
2年前
研究类型
Interventional
性别
All

研究者

发起方
Cancer Research Center, Kanazawa University

入排标准

入选标准

  • 未提供

排除标准

  • Within 4 weeks after the final administration of a cytotoxic anticancer agent.Allowable enrollment when a 7\-day washout is completed after the final administration of an EGFR\-TKI. Surgery of a primary tumor or to the mediastinum must be completed at least 6 months before the onset of protocol treatment. Radiotherapy to the lungs considered necessary at the time of study entry or in the near future. Having an interstitial lung disease (including acute pulmonary disorder, interstitial pneumonia, and drug inducibility) or having a history thereof. Having radiation pneumonitis or having a history thereof. Having a large volume of or uncontrollable pleural effusion, ascites, or pericardial effusion Detection of known EGFR\-TKI resistance acquired by mutations of the genes, e.g., T790M. Suffering from a severe or poorly controlled systemic disease (e.g., unstable or decompensated respiratory disease, heart disease, renal disease, and liver disease)

结局指标

主要结局

未指定

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