临床试验/NL-OMON42416

NL-OMON42416已完成不适用

A first-in-human, randomized, double-blind, placebo-controlled, single ascending dose and multiple ascending dose study to investigate the safety, tolerablility, pharmacokinetics (including food and gender effect), and pharmacodynamics of LNP1955 in healthy subjects. - LNP1955 Single and multiple ascending dose study.

upin Limited0 个研究点目标入组 66 人开始时间: 待定最近更新: 2024年4月23日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方
入组人数: 66

研究概览入排标准研究者记录与标识符相似试验

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 volunteers
•18-65 yrs, inclusive
•BMI: 18.0-32.0 kg/m2, inclusive

排除标准

•Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. In case of participation in another drug study within 90 days before the start of this study or being a blood donor within 60 days from the start of the study. In case of donating more than 1.5 liters of blood in the 10 months prior the start of this study.

研究者

发起方

upin Limited

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