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临床试验/JPRN-jRCT2080223524
JPRN-jRCT2080223524已完成3 期

Double-masked, Comparison Study of DE-114A Ophthalmic Solution in Patients With Allergic Conjunctivitis - Phase 3, Confirmatory Study

SANTEN PHARMACEUTICAL CO., LTD.0 个研究点目标入组 68 人开始时间: 2017年5月15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
68

研究概览

简要总结

The superiority of DE-114A ophthalmic solution (equivalent to 2 times a day) to placebo ophthalmic solution and non-inferiority to 0.05% epinastine hydrochloride ophthalmic solution (equivalent to 4 times a day) were verified. No adverse drug reaction and no safety issues were observed.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 64age old(—)
性别
All

入选标准

  • Provided signed, written informed consent.
  • Has a positive result from an allergen-specific IgE antibody 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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