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临床试验/JPRN-jRCT2080222549
JPRN-jRCT2080222549未知3 期

A double-blind, placebo-control, randomized phase III study to evaluate the efficacy and safety of TAC-202 in patients with perennial allergic rhinitis

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 750 人开始时间: 2014年7月1日最近更新:
适应症

试验速览

阶段
3 期
入组人数
750

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
>= 18age old 至 <= 74age old(—)
性别
All

入选标准

  • Subjects who have been diagnosed with perennial allergic rhinitis and who have had related symptoms for 2 years or longer.
  • Subjects who showed positive in nasal provocation test with house dust disc.

排除标准

  • Subjects who previously developed anaphylaxis to antihistamine drugs, fexofenadine or ingredients of the investigational drug.
  • Subjects with any of the following complications that may hinder efficacy evaluation
  • - Vasomotor rhinitis, - Eosinophilic rhinitis, - Drug-induced rhinitis,
  • - Viral conjunctivitis, - Otitis media,
  • - Others (acute/chronic rhinitis, hypertrophic rhinitis, sinusitis, nasal polyps, repetitive nasal hemorrhage, treatment-requiring nasal septal deviation, etc.)

研究者

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