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临床试验/JPRN-jRCT2080223566
JPRN-jRCT2080223566已完成3 期

A long-term Study of DE-114A Ophthalmic Solution in Patients with Allergic Conjunctivitis - Phase 3

SANTEN PHARMACEUTICAL CO., LTD.0 个研究点目标入组 121 人开始时间: 2017年6月22日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
121

研究概览

简要总结

DE-114A ophthalmic solution was instilled twice a day (morning and evening) for 8 weeks in subjects with allergic conjunctivitis. As a result, the safety and efficacy of long-term administration were confirmed.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 12age old 至 ot applicable(—)
性别
All

入选标准

  • Provided signed, written informed consent.
  • Has a positive result from a Type I allergy test.

排除标准

  • Eye disease other than allergic conjunctivitis is present and requires treatment.
  • Females who are pregnant, nursing or planning a pregnancy, or females of childbearing potential who are not using a reliable method of contraception.

研究者

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