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临床试验/EUCTR2004-002823-42-IT
EUCTR2004-002823-42-IT进行中(未招募)不适用

A multicentre, double-blind, parallel, randomized, placebo-controlled study Evaluation of the efficacy and safety of Levocetirizine 5 mg and Desloratadine 5 mg administered orally as capsules once daily, in the morning, over 2 weeks in patients suffering from Allergic Rhinitis AR

CB PHARMA0 个研究点目标入组 729 人开始时间: 2006年1月5日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
729

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 未提供

研究者

发起方
CB PHARMA

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A multicentre, double-blind, parallel, randomized, placebo-controlled study :Evaluation of the efficacy and safety of Levocetirizine 5 mg and Desloratadine 5 mgadministered orally as capsules once daily, in the morning, over 2 weeks in patientssuffering from Seasonal Allergic Rhinitis (SAR) due to grass polleAllergic Rhinitis (AR)MedDRA version: 7.1Level: LLTClassification code 10001723
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A multicentre, double-blind, parallel, randomized,... | 临床试验