NL-OMON46064已完成不适用
A single-center, randomized, double-blind, two-period cross-over study to investigate the effect of a single intravenous dose of rifampicin on the pharmacokinetics of ACT-246475 in healthy subjects. - CS0310 (ID-076-106)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
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
- 18 至 99（—）
入选标准
- •Healthy male and female subjects aged between 18 and 65 years (inclusive) with a Body mass index (BMI) of 18.0 to 30.0 kg/m2 (inclusive) at Screening.;Further inclusion criteria can be found in the protocol section 3.2.2
排除标准
- •1. Previous exposure to ACT-246475.
- •2. Previous exposure to rifampicin within 3 months prior to Screening.
- •3. Known hypersensitivity to P2Y12 receptor antagonists or rifampicin or to any of the rifamycins, or any of their excipients. ;Further exclusion criteria can be found in the protocol section 3.2.3.
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