Efficacy and safety of olopatadine-mometasone combination nasal spray for the treatment of seasonal allergic rhinitis

被引:44
作者
Gross, Gary N. [1 ]
Berman, Gary [2 ]
Amar, Niran J. [3 ]
Caracta, Cynthia F. [4 ]
Tantry, Sudeesh K. [4 ]
机构
[1] Pharmaceut Res & Consulting Inc, Dallas, TX USA
[2] Clin Res Inst Inc, Minneapolis, MN USA
[3] Allergy Asthma Res Inst, Waco, TX USA
[4] Glenmark Pharmaceut Inc, Paramus, NJ USA
关键词
QUALITY-OF-LIFE; AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE; INTRANASAL FORMULATION; DOUBLE-BLIND; PHARMACOKINETICS; MP29-02; THERAPY; GSP301; ONSET;
D O I
10.1016/j.anai.2019.03.017
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: GSP301 nasal spray is a fixed-dose combination of olopatadine hydrochloride (antihistamine) and mometasone furoate (corticosteroid). Objective: To evaluate the efficacy and safety of GSP301 in patients with seasonal allergic rhinitis (SAR). Methods: In this double-blind study, eligible patients (>= 12 years of age) with SAR were randomized 1:1:1:1 to twice-daily GSP301 (665 mu g of olopatadine and 25 mu g of mometasone), olopatadine (665 mu g), mometasone (25 mu g), or placebo for 14 days. The primary end point-mean change from baseline in average morning and evening 12-hour reflective Total Nasal Symptom Score (rTNSS)-was analyzed via a mixed-effect model repeated measures (P < .05 was considered to be statistically significant). Additional assessments included average morning and evening 12-hour instantaneous TNSS (iTNSS), ocular symptoms, individual symptoms, onset of action, quality of life, and adverse events (AEs). Results: A total of 1176 patients were randomized. GSP301 provided statistically significant and clinically meaningful rTNSS improvements vs placebo (least squares mean difference, -1.09; 95% CI, -1.49 to -0.69; P < .001) and vs olopatadine (P = .03) and mometasone (P = .02). Similar significant improvements in iTNSS were also observed with GSP301 (P <. 05 for all). Furthermore, GSP301 significantly improved overall ocular symptoms, individual nasal and ocular symptoms, and quality of life vs placebo (P <= .001 for all). Onset of action for GSP301 was observed within 15 minutes and was maintained at all subsequent timepoints. Treatment-emergent AEs occurred in 15.6%, 12.6%, 9.6%, and 9.5% of patients in the GSP301, olopatadine, mometasone, and placebo groups, respectively. Conclusion: GSP301 is efficacious and well tolerated vs placebo for treating SAR-associated nasal and ocular symptoms, with a rapid onset of action of 15 minutes in adult and adolescent patients 12 years and older. (C) 2019 American College of Allergy, Asthma & Immunology.
引用
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页码:630 / +
页数:12
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