NL-OMON52052招募中不适用
PHARMACOKINETICS OF APREPITANT, DEXAMETHASONE AND THEIR INTERACTION IN PATIENTS WITH CHEMOTHERAPY INDUCED NAUSEA AND VOMITING - PHARMACOKINETICS OF APREPITANT, DEXAMETHASONE AND THEIR INTERACTIO
Antoni van Leeuwenhoek Ziekenhuis0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 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
- 年龄范围
- 18 至 99（—）
入选标准
- •1. Planned to receive chemotherapy intravenously as regular treatment (standard
- •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 (appendix 2);
排除标准
- •See inclusion criteria
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