跳至主要内容
临床试验/CTRI/2020/04/024680
CTRI/2020/04/024680Other3 期

A Phase III, Multicenter, Sham-Controlled, Randomized, Double-Masked Study Assessing the Efficacy and Safety of Intravitreal Injections of 440 µg DE-109 for the Treatment of Active, Non-Infectious Uveitis of the Posterior Segment of the Eye. - LUMINA

Santen Incorporated0 个研究点目标入组 47 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
Other
入组人数
47

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

入选标准

  • Non-Infectious Active Uveitis of the Posterior Segment

排除标准

  • Females who are pregnant, nursing or planning a pregnancy.
  • Confirmed or suspected infectious uveitis.

研究者

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