首页> 外文期刊>Allergology international: official journal of the Japanese Society of Allergology >A Double-Blind Non-inferiority Clinical Study of Montelukast, a Cysteinyl Leukotriene Receptor 1 Antagonist, Compared with Pranlukast in Patients with Seasonal Allergic Rhinitis
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A Double-Blind Non-inferiority Clinical Study of Montelukast, a Cysteinyl Leukotriene Receptor 1 Antagonist, Compared with Pranlukast in Patients with Seasonal Allergic Rhinitis

机译:半胱氨酸半胱氨酸三烯受体1拮抗剂孟鲁司特与普仑司特对季节性变应性鼻炎患者的双盲非劣效性临床研究

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Background: During the course of development of montelukast, a cysteinyl leukotriene receptor 1 antagonist, for treatment of seasonal allergic rhinitis, a double-blind, non-inferiority study was carried out to evaluate the efficacy and safety of montelukast 5 mg and 10 mg compared with pranlukast 450 mg, which has a similar mechanism of action.Methods: Montelukast 5 mg, 10 mg or pranlukast 450 mg and the corresponding placebo were orally administered to patients with seasonal allergic rhinitis three times a day for 2 weeks. Non-inferior efficacy of montelukast 5 mg and 10 mg to pranlukast 450 mg was investigated by the change from the baseline in the composite nasal symptoms scores over the 2-week treatment period.Results: Montelukast 5 mg, 10 mg once daily and the pranlukast 450 mg/day showed significant improvements in the change from the baseline in the composite, daytime and nighttime nasal symptom scores, and the improvement lasted for 2 weeks. Montelukast 5 mg and 10 mg were non-inferior to pranlukast 450 mg in the change from the baseline in the composite nasal symptoms scores. The incidence rates of adverse experiences and drug-related adverse experiences were not significantly different among the three treatment groups. Conclusions: The results indicate that administration of montelukast 5 mg and 10 mg once daily are potent alternatives for the treatment of seasonal allergic rhinitis and demonstrated that the efficacy and the safety profiles are comparable with pranlukast 450 mg/day.
机译:背景:在半胱氨酸白三烯受体1拮抗剂孟鲁司特的开发过程中,为了治疗季节性变应性鼻炎,进行了一项双盲,非劣效性研究,以评估孟鲁司特5 mg和10 mg的疗效和安全性方法:将普鲁司特5 mg,普鲁司特450 mg,10 mg或普鲁司特450 mg以及相应的安慰剂与季节性过敏性鼻炎患者一起口服,每天两次,共3周,共2周。通过在2周的治疗期内复合鼻症状评分相对于基线的变化,研究了孟鲁司特5 mg和10 mg对普仑司特450 mg的非劣效性。结果:孟鲁司特5 mg,每天10 mg一次,普仑司特450 mg /天显示出复合物,白天和夜间鼻部症状评分相对于基线的变化有显着改善,并且持续了2周。孟鲁司特5 mg和10 mg在鼻综合症状评分相对于基线的变化中不逊于普鲁司特450 mg。在三个治疗组之间,不良反应和药物相关不良反应的发生率没有显着差异。结论:结果表明,每天一次给予孟鲁司特5 mg和10 mg是治疗季节性变应性鼻炎的有效替代方法,并证明其有效性和安全性与普鲁司特450 mg / day相当。

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