jRCT2080222394已完成1 期
A Phase I, Dose Escalation Study Evaluating the Safety, Tolerability and Pharmacokinetics of TAS-116 in Patients with Advanced Solid Tumors.
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 干预模型
- Open-label, phase I study
- 主要目的
- Treatment Purpose
入排标准
- 年龄范围
- 20age old over 至 No limit（—）
- 性别
- All
入选标准
- •Signed, written informed consent.
- •Histologically or cytologically confirmed solid tumor.
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.
排除标准
- •Investigational drug therapy within 21 days prior to enrollment.
- •Radiotherapy within 21 days prior to enrollment.
- •Received extensive prior radiotherapy on more than 30% of bone marrow.
- •Females who are pregnant or breastfeeding.
- •Serious complications.
结局指标
主要结局
-
safety Safety CTCAE (ver.4.03)
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
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