Fluticasone furoate nasal spray is effective and well tolerated for perennial allergic rhinitis in adolescents and adults

被引:14
作者
Given, John T. [1 ]
Cheema, Amarjit S. [2 ]
Dreykluft, Tilman
Stillerman, Allan [3 ]
Silvey, MaryJane [4 ]
Wu, Wei [4 ]
Snowise, Neil G. [5 ]
Philpot, Edward [4 ]
机构
[1] Allergy & Resp Ctr, Canton, OH 44718 USA
[2] Alpha Med Res Inc, Mississauga, ON, Canada
[3] Clin Res Inst Inc, Plymouth, MN USA
[4] GlaxoSmithKline Inc, Res Triangle Pk, NC USA
[5] GlaxoSmithKline Inc, Uxbridge, Middx, England
关键词
QUALITY-OF-LIFE; OCULAR SYMPTOMS; INTRANASAL CORTICOSTEROIDS; SIGNIFICANTLY IMPROVES; EYE SYMPTOMS; RHINOCONJUNCTIVITIS; QUESTIONNAIRE; EFFICACY; SAFETY; PROPIONATE;
D O I
10.2500/ajra.2010.24.3534
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background: Fluticasone furoate nasal spray (FFNS), an intranasal corticosteroid, has been shown to be effective in perennial allergic rhinitis in randomized, double-blind, placebo-controlled studies but has been less extensively studied in perennial allergic rhinitis than seasonal allergic rhinitis. This study was designed to evaluate the efficacy and safety of FFNS in perennial allergic rhinitis in adolescents and adults >= 12 years of age. Methods: In this randomized, double-blind, placebo-controlled, parallel-group study (FFU111439), patients >= 12 years old with perennial allergic rhinitis received FFNS, 110 micrograms (n = 160), or placebo (n = 155) q.d. for 4 weeks. Results: Over the entire treatment period, FFNS was significantly (p < 0.05) more effective than placebo with respect to mean changes from baseline in daily reflective total nasal symptoms (primary end point), morning and evening reflective total nasal symptoms, daily reflective individual nasal symptoms, morning predose instantaneous total and individual nasal symptoms, and morning and evening peak nasal inspiratory flow. FFNS did not show a statistically significant difference from placebo in comparisons of ocular symptom measures. Clinically meaningful improvement versus placebo was observed on the Rhinoconjunctivitis Quality of Life Questionnaire with Standardised Activities overall score. Adverse events reported in >3% of patients in a treatment group and reported more frequently with FFNS than placebo were epistaxis (15% FFNS, 8% placebo) and nasopharyngitis (5% FFNS, 1% placebo). Conclusion: Once-daily FFNS was well tolerated and more effective than placebo at improving nasal symptoms of perennial allergic rhinitis in adolescents and adults >= 12 years of age.
引用
收藏
页码:444 / 450
页数:7
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