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临床试验/JPRN-UMIN000018866
JPRN-UMIN000018866已完成未知

Phase IIb study of SNJ-1656; A dose-response study in patients with primary open angle glaucoma or ocular hypertension - A dose-response study of SNJ-1656 in patients with primary open angle glaucoma or ocular hypertension

Senju Pharmaceutical co.,ltd.0 个研究点目标入组 180 人开始时间: 2015年8月31日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
180

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Active retinal disease 2)History of keratorefractive surgery or filtering surgery 3)History of trabeculotomy or laser trabeculoplasty in the study eye 4)Highly visual field loss 5)Corneal abnormalities that would preclude accurate readings with an applanation tonometer 6)Ocular surgery within 90 days 7)Use of contact lenses 8)Any active ocular disease other than glaucoma or OH 9)Uncontrolled systemic disease (eg, hepatic, renal, cardiovascular or endocrine system disease) 10)Women who were pregnant, nursing or who were of childbearing potential, or planning a pregnancy

研究者

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