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临床试验/NL-OMON32022
NL-OMON32022已完成不适用

A double-blind, randomized, placebo-controlled study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single ascending oral doses of ASP2905 in healthy young males, including an open-label two-period randomized crossover study to compare the pharmacokinetics under fasted and fed conditions - ASP2905 SAD/food effect study

Astellas Pharma0 个研究点目标入组 68 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
已完成
入组人数
68

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 male subject, aged 18-50 years inclusive.

排除标准

  • current clinically significant diseases or conditions or any clinical significant diseases or conditions in medical history.

研究者

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