JPRN-jRCT2080222600未知1 期
A PHASE I, OPEN-LABEL, NON-RANDOMIZED, DOSE-ESCALATING, SAFETY, TOLERABILITY, PHARMACOKINETIC, AND EFFICACY STUDY OF TAS-121 IN PATIENTS WITH ADVANCED NON-SMALL CELL LUNG CANCER (NSCLC)
适应症
试验速览
- 阶段
- 1 期
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
- •1. Provided written informed consent for treatment.
- •2. Male or female >=20 years at enrollment.
- •3. Histologically or cytologically confirmed NSCLC.
- •4. Have a previous treatment with a single-agent EGFR TKI.
- •5. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 at time of patient's allocation.
排除标准
- 未提供
研究者
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