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1 with moderate-to-severe rhinitis than FP and azelastine.
2 3]) more than FP (-5.1 [SD, 4.9], P < .001), azelastine (-4.4 [SD, 4.8], P < .001), or placebo (-3.0
4 bitor of mast cell degranulation, but not by azelastine, a histamine receptor 1 antagonist, or by ket
5 efficacy of MP29-02 (a novel formulation of azelastine and fluticasone propionate [FP]) in patients
7 ess commonly used in clinical practice (i.e. azelastine, chlorpheniramine, hydroxyzine, and ketotifen
14 valuate the corticosteroid-sparing effect of azelastine in patients with chronic bronchial asthma.
15 loratadine), intranasal antihistamines (eg, azelastine, olopatadine), and intranasal corticosteroids
16 atadine) or an intranasal antihistamine (eg, azelastine, olopatadine), whereas patients with persiste
17 atment with histamine receptor-1 antagonist, azelastine prevented the early effect of nasal secretion
19 otal of 193 subjects received either 6 mg of azelastine twice per day or placebo (in a 2:1 ratio) in
20 n inhaled corticosteroids (4.9 puffs/day for azelastine versus 3.1 puffs/day for placebo; p < or = 0.
21 aseline level (53 and 31%, respectively, for azelastine versus 34 and 14%, respectively, for placebo;