NL-OMON20649尚未招募不适用
Pharmacokinetics of- and interaction between aprepitant and dexamethasone
Princess Maxima Center for pediatric oncology0 个研究点目标入组 20 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •1.Planned to receive chemotherapy intravenously as regular treatment (standard of care);
- •2.Receiving dexamethasone with or without aprepitant as standard of care
- •3.Receiving the chemotherapy and anti-emetics during hospitalized treatment.
- •4.Age =18;
- •5.Signed Informed consent form (ICF) prior to participation in the study;
- •6.Able and willing to undergo blood draw for the study (two different days, 6 times per day) and does not have any condition that makes participation disadvantageous;
- •7.For women: not pregnant
- •8.No use of strong CYP3A4 substrates or inhibitors within 7 days or CYP3A4 inducers within 30 days of treatment;
排除标准
- •See inclusion criteria
研究者
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