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临床试验/JPRN-jRCT2080222986
JPRN-jRCT2080222986未知1 期

A Randomized, Double-blind, Placebo-controlled, 2-Part Study of Orally Administered ALS-008176 to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Dosing and Multiple Ascending Dosing in Infants Hospitalized With Respiratory Syncytial Virus (RSV) Infection

Janssen Pharmaceutical K.K.0 个研究点目标入组 24 人开始时间: 2015年10月14日最近更新:

试验速览

阶段
1 期
入组人数
24

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
>= 至 <= 1age old(—)
性别
All

入选标准

  • Male or female subjects, 1-12 months old, hospitalized with RSV infection, in otherwise good health

排除标准

  • Prematurity
  • Receiving invasive endotracheal mechanical ventilation
  • Poorly functioning gastrointestinal tract
  • Anticipated to be discharged from the hospital in <24 hours from the time of randomization
  • Prior exposure to palivizumab

研究者

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A Study of ALS-008176 in Infants Hospitalized With... | 临床试验