NL-OMON48259已完成不适用
Interventional, randomized, double-blind, sequential-group, placebo-controlled, single-ascending-oral-dose study investigating the safety, tolerability, pharmacokinetic, and pharmacodynamic properties of Lu AF88434 and open-label crossover study to investigate the intra-individual variability, metabolic profile, and effect of food on Lu AF88434 in healthy young men - 18144A Lundbeck (190100)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 84
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 young non-smoking men with a body mass index (BMI) *
- •18.5kg/m2 and *30kg/m2 at the Screening Visit.
- •Please refer to the protocol for more inclusion criteria.
排除标准
- •The subject has any concurrent disorder that may affect the particular target
- •or absorption, distribution, or elimination of the IMP.
- •Please refer to the protocol for more exclusion criteria.
研究者
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