Abstract | BACKGROUND: Moderate-to-severe allergic rhinitis (AR) is a challenge to treat, with many patients using multiple therapies and achieving limited symptom control. More effective therapies must be developed and tested in well-controlled, randomized, prospective studies with a direct comparison to current standards. OBJECTIVES: METHODS: Three thousand three hundred ninety-eight patients (≥12 years old) with moderate-to-severe SAR were enrolled into 3 multicenter, randomized, double-blind, placebo- and active-controlled, parallel-group trials (MP4002 [NCT00651118], MP4004 [NCT00740792], and MP4006 [NCT00883168]). Each trial was conducted for 14 days during different allergy seasons. The primary efficacy variable was the sum of the morning and evening change from baseline in reflective total nasal symptom score (range, 0-24) over the treatment period. Outcomes for the meta-analysis included efficacy according to disease severity and time to response in relevant responder criteria. RESULTS: In the meta-analysis MP29-02 reduced the mean reflective total nasal symptom score from baseline (-5.7 [SD, 5.3]) more than FP (-5.1 [SD, 4.9], P < .001), azelastine (-4.4 [SD, 4.8], P < .001), or placebo (-3.0 [SD, 4.2], P < .001). This benefit was observed from the first day of assessment, with improvement in each individual nasal symptom, even in the patients with the most severe disease. MP29-02 achieved response consistently days earlier and showed greater efficacy in patients with moderate-to-severe rhinitis than FP and azelastine. CONCLUSIONS:
MP29-02 represents a novel therapy that demonstrated superiority to 2 first-line therapies for AR. Patients with moderate-to-severe SAR achieved better control, and their symptoms were controlled earlier with MP29-02 than with recommended medications according to guidelines.
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Authors | Warner Carr, Jonathan Bernstein, Phil Lieberman, Eli Meltzer, Claus Bachert, David Price, Ullrich Munzel, Jean Bousquet |
Journal | The Journal of allergy and clinical immunology
(J Allergy Clin Immunol)
Vol. 129
Issue 5
Pg. 1282-1289.e10
(May 2012)
ISSN: 1097-6825 [Electronic] United States |
PMID | 22418065
(Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Copyright | Copyright © 2012 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved. |
Chemical References |
- Androstadienes
- Drug Combinations
- MP29-02
- Phthalazines
- Fluticasone
- azelastine
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Topics |
- Administration, Intranasal
- Adult
- Androstadienes
(administration & dosage, adverse effects, chemistry)
- Disease Progression
- Drug Combinations
- Female
- Fluticasone
- Guidelines as Topic
- Humans
- Male
- Middle Aged
- Nasal Obstruction
(etiology, physiopathology, prevention & control)
- Phthalazines
(administration & dosage, adverse effects, chemistry)
- Rhinitis, Allergic, Seasonal
(complications, drug therapy, physiopathology)
- Seasons
- Severity of Illness Index
- Young Adult
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