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临床试验/JPRN-jRCT2080223031
JPRN-jRCT2080223031未知1 期

Phase 1, Open-label Study to Assess the Safety, Tolerability, and Pharmacokinetics of DS-1123a in Subjects with Advanced Solid Tumors

DAIICHISANKYO Co.,Ltd.0 个研究点目标入组 27 人开始时间: 2015年11月30日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
27

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Advanced solid tumor that is refractory to standard treatment, or for which no standard treatment is available.
  • -ECOG Performance Status (PS) of 0 or 1

排除标准

  • -Have any of the following concomitant disease or had the history of having following disease within 6 months before enrollment:
  • Cardiac failure (NYHA >= ClassIII), myocardial infarction, cerebral infarction, unstable angina, arrhythmia requiring treatment, coronary-artery/peripheral artery bypass surgery, cerebrovascular disease, pulmonary thromboembolism, deep-vein thrombosis or clinically severe thromboembolic events, or clinically severe pulmonary disease (eg, interstitial pneumonia, pulmonary fibrosis, radiation pneumonia, drug induced pneumonia)
  • -Severe or uncontrolled concomitant disease.
  • -Clinically active brain metastases defined as symptomatic or requiring treatment.

研究者

发起方
DAIICHISANKYO Co.,Ltd.

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