Detailed Information

Cited 0 time in webofscience Cited 16 time in scopus
Metadata Downloads

A Randomized, Multicenter, Double-blind, Phase III Study to Evaluate the Efficacy on Allergic Rhinitis and Safety of a Combination Therapy of Montelukast and Levocetirizine in Patients With Asthma and Allergic Rhinitis

Authors
Kim, Mi-KyeongLee, Sook YoungPark, Hae-SimYoon, Ho JooKim, Sang-HaCho, Young JooYoo, Kwang-HaLee, Soo-KeolKim, Hee-KyooPark, Jung-WonPark, Heung-WooChung, Jin-HongChoi, Byoung WhuiLee, Byung-JaeChang, Yoon-SeokJo, Eun-JungLee, Sang-YeubCho, You SookJee, Young-KooLee, Jong-MyungJung, JinaPark, Choon-Sik
Issue Date
Jul-2018
Publisher
Excerpta Medica, Inc.
Keywords
allergic rhinitis; asthma; clinical trial; fixed-dose combination; levocetirizine; montelukast
Citation
Clinical Therapeutics, v.40, no.7, pp 1096 - 1107
Pages
12
Journal Title
Clinical Therapeutics
Volume
40
Number
7
Start Page
1096
End Page
1107
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/5832
DOI
10.1016/j.clinthera.2018.04.021
ISSN
0149-2918
1879-114X
Abstract
Purpose: The aim of this study was to evaluate the efficacy and safety of a fixed-dose combination of montelukast and levocetirizine in patients with perennial allergic rhinitis with mild to moderate asthma compared with the efficacy and safety of montelukast alone. Methods: This study was a 4-week, randomized, multicenter, double-blind, Phase III trial. After a 1 week placebo run-in period, the subjects were randomized to receive montelukast (10 mg/day, n = 112) or montelukast (10 mg/day)/levocetirizine (5 mg/day) (n = 116) treatment for 4 weeks. The primary efficacy end point was mean daytime nasal symptom score. Other efficacy end points included mean nighttime nasal symptom score, mean composite symptom score, overall assessment of allergic rhinitis by both subjects and physicians, forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), FEV1/FVC, asthma control test score, and the frequency of rescue medication used during the treatment period. Findings: Of 333 patients screened for this study, 228 eligible patients were randomized to treatment. The mean (SD) age of patients was 43.32 (15.02) years, and two thirds of subjects were female (66.67%). The demographic characteristics were similar between the treatment groups. Compared with the montelukast group, the montelukast/levocetirizine group reported significant reductions in mean daytime nasal symptom score (least squares mean [SE] of combination vs montelukast, -0.98 [0.06] vs -0.81 [0.06]; P = 0.045). For all other allergic rhinitis efficacy end points, the montelukast/levocetirizine group showed greater improvement than the montelukast group. Similar results were observed in overall assessment scores and in FEV1, FVC, FEV1/FVC, and asthma control test score changes from baseline for the 2 treatment groups. Montelukast/levocetirizine was well tolerated, and the safety profile was similar to that observed in the montelukast group. (C) 2018 The Authors. Published by Elsevier Inc.
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Internal Medicine > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE