가장 나다운 순간이 계속되도록! 알레그라^®

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9. 2023 소비자가 뽑은 올해의 브랜드대상, 2년 연속 수상 (알레르기비염 치료제 부문) 사단법인 한국방송신문연합회 주관

10. Brożek JL et al. Allergic Rhinitis and its Impact on Asthma (ARIA) guidelines-2016 revision. J ALLERGY CLIN IMMUNOL. 2017.140(4);950-958

[Study Design¹] This was a multinational, multicentre, double-blind, parallel group, randomized, placebo-controlled study. Following a placebo run-in phase of 3±7 days (the baseline period), patients with SAR were randomized to receive one capsule of either fexofenadine HCl 120mg(n=232), loratadine 10mg(n=228), or placebo(n=225), once each morning for 14 days. The primary efficacy parameter was the change in the mean 24-h reflective TSS during the double-blind treatment period from that during the baseline period.

[Study Design⁶] This study was of a randomized, placebo-controlled, double-blind, parallel design. The purpose of this study was to characterize the time to onset of clinically important relief of symptoms of allergic rhinitis in subjects taking single doses of either 60 mg or 120 mg fexofenadine HCl, or placebo, after exposure to ragweed pollen in a controlled environment. Other objectives were to assess the efficacy and safety of single doses of fexofenadine HCl.

[Study Design⁸] A multicenter, double-blind, parallel-group, placebo-controlled trial compared the efficacy and safety of fexofenadine HCl (120 and 180 mg administered once daily) and cetirizine (10 mg once daily) in the treatment of seasonal allergic rhinitis. The primary efficacy variable was the change in mean 24-hour reflective TSS during the treatment period in relation to the single blind placebo lead-in phase.