跳至主要内容
临床试验/JPRN-jRCT2080221806
JPRN-jRCT2080221806未知2 期

Phase II/III Clinical Trial of TO-203 -Efficacy and Safety Trial in Patients with HDM-induced Rhinitis

TORII PHARMACEUTICAL CO., LTD.0 个研究点目标入组 900 人开始时间: 2012年5月29日最近更新:
适应症

试验速览

阶段
2 期
入组人数
900

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
>= 12age old 至 <= 64age old(—)
性别
All

入选标准

  • (1) HDM-specific IgE antibodies >= Class 3
  • (2) Positive on HDM nasal provocation test
  • (3) Medical history of treatment for HDM-induced rhinitis
  • (4) Moderate or severe symptoms of HDM-induced rhinitis

排除标准

  • (1) Specific IgE antibodies >= Class 5 any of the following: cedar, cypress, alder, cocksfoot, ragweed, mugwort, Japanese hop, cockroach, Candida, Aspergillus, Alternaria, dog hair, or cat hair
  • (2) Allergic rhinitis symptoms with class 2 to 4 in the specific IgE antibodies any of the following: cocksfoot, ragweed, mugwort, Japanese hop, cockroach, Candida, Aspergillus, Alternaria, dog hair, or cat hair
  • (3) Class 2 to 4 in the specific IgE antibody to dog hair or cat hair, and no rhinitis symptoms, but constantly exposed to the relevant animal (e.g., pet parenting at home, working at a pet shop)
  • (4) Patients who received immunotherapy with HDM allergen-containing products (e.g., house dust) for at least 1 month during 5 years before the first day of observation.
  • (5) Patients who are on immunotherapy other than HDM allergen-containing products on the first day of observation.

研究者

相似试验