JPRN-jRCT2080220617未知1 期
A Phase I, Open-Label, Dose-Escalation Study to Assess the Safety and Tolerability of AZD0530 in Patients With Advanced Solid Malignancies
适应症
试验速览
- 阶段
- 1 期
- 发起方
- AstraZeneca
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
- •Accepts Healthy Volunteers: No
- •-Histologically or cytologically confirmed advanced carcinoma / solid tumour of known primary site, which is refractory to standard therapies or for which no standard therapy exists.
- •-World Health Organisation (WHO) performance status 0 to 2.
- •-Life expectancy of at least 12 weeks.
排除标准
- •-Inadequate bone marrow reserve.
- •-Inadequate liver function, renal function or low hemoglobin.
- •-Unresolved toxicity from anti-cancer therapy.
研究者
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