跳至主要内容
临床试验/JPRN-jRCT2080224816
JPRN-jRCT2080224816已完成2 期

A randomized, double-masked, placebo-controlled study of DE-127 ophthalmic solution in subjects with myopia - A Phase II/III, Confirmatory Study

Santen Pharmaceutical co.,Ltd0 个研究点目标入组 288 人开始时间: 2019年8月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
288

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
>= 5age old 至 <= 15age old(—)
性别
All

入选标准

  • Written informed consent from legally acceptable representative and assent from subject have been obtained.
  • - Cycloplegic objective spherical equivalent -1.0 to -6.0 D
  • - Active myopia progression with vision acuity test

排除标准

  • - Patients who previously used contact lenses and/or treatments for reducing myopia progression.
  • - Patients who previously participated in a clinical trial of DE-127 ophthalmic solution.
  • - Other patients who are inappropriate as participants in this study in the opinion of the investigator or subinvestigator.

研究者

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