- Open Access
Escaping the trap of allergic rhinitis
Clinical and Molecular Allergy volume 13, Article number: 17 (2015)
Rhinitis is often the first symptom of allergy but is frequently ignored and classified as a nuisance condition. Ironically it has the greatest socioeconomic burden worldwide caused by its impact on work and on daily life.
However, patients appear reticent to seek professional advice, visiting their doctor only when symptoms become ‘intolerable’ and often when their usual therapy proves ineffective.
Clearly, it’s time for new and more effective allergic rhinitis treatments.
MP29-02 (Dymista®; Meda, Solna, Sweden) is a new class of medication for moderate to severe seasonal and perennial allergic rhinitis if monotherapy with either intranasal antihistamine or intranasal corticosteroids is not considered sufficient.
MP29-02 is a novel formulation of azelastine hydrochloride (AZE) and fluticasone propionate (FP). It benefits not only from the incorporation of two active agents, but also from a novel formulation; its lower viscosity, smaller droplet size, larger volume (137 μl) and wider spray angle ensure optimal coverage of, and retention on the nasal mucosa and contribute to its clinical efficacy.
In clinical trials, patients treated with MP29-02 experienced twice the symptom relief as those treated with FP and AZE, who in turn exhibited significantly greater symptom relief than placebo-patients. Indeed, the advantage of MP29-02 over FP was approximately the same as that shown for FP over placebo. The advantage of MP29-02 was particularly evident in those patients for whom nasal congestion is predominant, with MP29-02 providing three times the nasal congestion relief of FP (p = 0.0018) and five times the relief of AZE (p = 0.0001). Moreover, patients treated with MP29-02 achieved each and every response up to a week faster than those treated with FP or AZE alone and in real life 1 in 2 patients reported the perception of well-controlled disease after only 3 days. MP29-02’s superiority over FP was also apparent long-term in patients with perennial allergic rhinitis or non-allergic rhinitis, with statistical significance noted from the first day of treatment, with treatment difference maintained for a full year.
Taken together, these data suggest that MP29-02 may improve the lives of many of our patients, enabling them to finally escape the allergic rhinitis trap.
The allergy trap
In Europe 150 million people are trapped by allergy [1, 2]. One out of 3 children are allergic  and 50 % of Europeans will suffer from allergy within the next 10 years ! Not surprisingly asthma and anaphylaxis get the lion’s share of medical and media attention, due to the possibility of fatality. Consequently other allergic diseases, such as allergic rhinitis (AR), are frequently ignored and often trivialised as a nuisance condition.
Ironically, AR accounts for the greatest socioeconomic burden worldwide, higher than that induced by asthma, diabetes and heart disease . The knock on cost is enormous, €2 billion euros in Sweden alone . Furthermore, patients with AR are daily burdened with the misery of nasal and ocular symptoms, making them tired, miserable and irritable . No aspect of patients’ lives, from sleep to cognitive functions, escapes the rhinitis touch [7, 8], including an increased risk of road traffic accidents . Considering that AR is also a risk factor for asthma , the time to ignore AR is long past.
However, patients appear reluctant to seek professional advice until their symptoms become ‘intolerable’ . Unfortunately, many physicians under-estimate AR severity and under-treat it . Patients, therefore, struggle to alleviate their misery, frequently use over the counter drugs and homeopathic remedies [13, 14]. Notably, many patients remain symptomatic despite optimal treatment  or multiple therapy usage [16, 17], the latter not endorsed by ARIA due to limited supporting evidence [18–20].
Escaping the trap
Clearly, it’s time for new and more effective AR treatments. The last major breakthrough in symptomatic treatment was the introduction of intranasal corticosteroids (INS) over 50 years ago, now recommended as first line treatment for moderate/severe AR [21–23].
MP29-02 (Dymista®; Meda, Solna, Sweden), launched in the US in 2012 and in Europe in 2013, is a new class of medication (WHO code ATC R01AD58) for moderate to severe seasonal and perennial AR if monotherapy with either intranasal antihistamine or INS is not considered sufficient . MP29-02 is a novel intranasal formulation of azelastine hydrochloride (AZE) and fluticasone propionate (FP). It benefits from the incorporation of two active agents with broad pathologic coverage and complementary effects, but also from a novel formulation. MP29-02’s lower viscosity, smaller droplet size, larger volume (137 μl) and wider spray angle ensure optimal coverage of, and retention on, the nasal mucosa contributing to its efficacy .
The clinical development of MP29-02 has been a unique one for several reasons. Firstly it was the largest head to head development programme, to our knowledge, ever carried out in AR incorporating four 14-day seasonal AR (SAR) studies [26–28], and one long-term (52-week) study in patients with chronic rhinitis (i.e., perennial AR (PAR) and non-allergic rhinitis (NAR))  (4617 patients overall). In contrast to other AR drugs, MP29-02’s efficacy was compared not only with placebo, but also versus two first-line AR treatments; a clinically-relevant study design, since in real-life patients are not treated with placebo. The MP29-02 group experienced twice the nasal and ocular symptom relief as those treated with FP or AZE alone, with all active treatments providing significantly greater symptom relief than placebo [26–28]. Indeed, the advantage of MP29-02 over commercially-available FP was approximately the same as that shown for FP over placebo (Fig. 1) . MP29-02’s superiority over FP persisted long-term in patients with PAR and NAR, with statistical significance observed from the first day of treatment and sustained benefit established for a full year , without safety concerns .
In this 1-year, randomized, open-label, active-controlled, parallel-group study including more than 600 patients with allergic or non-allergic rhinitis, MP29-02 showed similar adverse events incidence (9.4 %) compared to FP (11.1 %), no evidence of late-occurring adverse events or of nasal mucosal ulcerations or septal perforations, no unusual or unexpected ocular examination findings and no clinically important laboratory findings or clinically important differences between groups in fasting AM serum cortisol levels after 12 months of treatment .
Secondly, patients recruited into the MP29-02 SAR trials [26–28] were among the most severe patients with a mean baseline reflective total nasal symptom score (rTNSS) of 19/24. They were required to have moderate to severe nasal congestion, the nasal symptom considered most bothersome  and often recalcitrant to treatment. These patients are usually excluded from AR clinical trials. The advantage of MP29-02 over FP and AZE was particularly evident in patients with nasal congestion predominantly, with MP29-02 providing three times the nasal congestion relief of FP (p = 0.0018) and five times the relief of AZE (p = 0.0001) (Fig. 2) . By comparison, FP or AZE induced the same level of congestion relief in these patients as placebo . This FP and AZE treatment failure helps to explain why many AR patients experience breakthrough symptoms and often express treatment dissatisfaction .
Thirdly, the efficacy of MP29-02 was assessed in a novel and clinically-relevant way by responder analyses, as suggested by the European Medicines Agency . Data showed that patients treated with MP29-02 achieved each and every response (from 30 to 90 % change from baseline in rTNSS) up to week faster than those treated with FP or AZE alone . It means something to patients and physicians (rather than symptom score change), enabling an estimation of the likelihood of achieving a substantial response or complete symptom relief, and when to expect that level of response. The responder analyses also identified an efficacy plateau for FP (i.e., ≥60 % response) and for AZE (i.e., ≥50 % response) above which these treatments did not significantly differ from placebo, again highlighting the unmet pharmacological need in AR and the insufficiency of currently considered first-line treatment options for many patients with moderate/severe disease. MP29-02 was significantly superior to placebo for all responses, and no plateau effect was observed .
Fourthly, by virtue of differently formulated active comparators, MP29-02’s development programme enabled observation of the effect of formulation on clinical efficacy. In one study  MP29-02 was compared to commercially-available comparators and in 3 studies  it was compared to FP and AZE made up in the MP29-02 formulation and delivered in the MP29-02 device. MP29-02’s treatment effect was consistent in all studies but the treatment difference was more marked in the study versus commercial comparators , since here the effect of formulation contributed to MP29-02’s efficacy. This may help to explain the over-additive effects of MP29-02 observed for several parameters (Fig. 2).
Finally, MP29-02’s clinical development programme has continued with a large (n = 1781) non-interventional real-life study , completing the continuum from efficacy to effectiveness. Assessment of effectiveness is crucial, since real-life studies include patients usually excluded from randomized controlled trials (RCTs; e.g., patients with co-morbid asthma, heart disease, diabetes, smokers, poorly compliant patients, etc.). Patients treated with MP29-02 in real-life experienced rapid symptom control, with 1 in 2 patients reporting the perception of well-controlled disease after only 3 days (Fig. 3) . Effectiveness was assessed using a visual analogue scale (VAS) which has been recommended by MACVIA-LR ARIA as the new language of AR control and will form the basis of the new AR guideline termed the AR integrated care pathway . The real-life response to MP29-02, was better than that observed in the RCTs, independent of disease severity or phenotype (i.e., PAR, SAR or PAR + SAR) .
MP29-02 provides significantly better nasal and ocular symptom relief than INS, which up to now has been considered the most effective treatment for AR. Clinical data analyses showed that, unlike other therapies, MP29-02 has no efficacy threshold, and continues to provide superior relief to established therapies regardless of patient type, season, symptom or severity. Its effectiveness has been proven in real life, with response rates even greater than those observed in controlled trials. Taken together, these data suggest that MP29-02 may improve the lives of many of our AR patients, enabling them to finally escape the AR trap.
Allergic Rhinitis and its Impact on Asthma
contres les MAladies Chronique pour un VIeillissement Actif
Non allergic rhinitis
Perennial allergic rhinitis
Randomized controlled trials
Seasonal allergic rhinitis
Visual analogue scale
European Academy of Allergy and Clinical Immunology (EAACI). Beware of Allergy Campaign. 2015. http://www.bewareofallergy.com/. Accessed 9 Feb 2015.
Calderon MA, Demoly P, Gerthvan WR, Bousquet J, Sheikh A, Frew A, et al. EAACI: A European Declaration on Immunotherapy. Designing the future of allergen specific immunotherapy. Clin Transl Allergy. 2012;2:20.
Global Allergy and Asthma European Network (GA2LEN). Call to action. 2015. http://www.ga2len.net/calltoaction.html. Accessed 9 Feb 2015.
Lamb CE, Ratner PH, Johnson CE, Ambegaonkar AJ, Joshi AV, Day D, et al. Economic impact of workplace productivity losses due to allergic rhinitis compared with select medical conditions in the United States from an employer perspective. Curr Med Res Opin. 2006;22:1203–10.
Hellgren J, Cervin A, Nordling S, Bergman A, Cardell LO. Allergic rhinitis and the common cold--high cost to society. Allergy. 2010;65:776–83.
Meltzer EO, Blaiss MS, Derebery MJ, Mahr TA, Gordon BR, Sheth KK, et al. Burden of allergic rhinitis: results from the Pediatric Allergies in America survey. J Allergy Clin Immunol. 2009;124:S43–70.
Valovirta E, Myrseth SE, Palkonen S. The voice of the patients: allergic rhinitis is not a trivial disease. Curr Opin Allergy Clin Immunol. 2008;8:1–9.
Walker S, Khan-Wasti S, Fletcher M, Cullinan P, Harris J, Sheikh A. Seasonal allergic rhinitis is associated with a detrimental effect on examination performance in United Kingdom teenagers: case-control study. J Allergy Clin Immunol. 2007;120:381–7.
Vuurman EF, Vuurman LL, Lutgens I, Kremer B. Allergic rhinitis is a risk factor for traffic safety. Allergy. 2014;69:906–12.
Shaaban R, Zureik M, Soussan D, Neukirch C, Heinrich J, Sunyer J, et al. Rhinitis and onset of asthma: a longitudinal population-based study. Lancet. 2008;372:1049–57.
Maurer M, Zuberbier T. Undertreatment of rhinitis symptoms in Europe: findings from a cross-sectional questionnaire survey. Allergy. 2007;62:1057–63.
Meltzer EO. Allergic rhinitis: the impact of discordant perspectives of patient and physician on treatment decisions. Clin Ther. 2007;29:1428–40.
Pitman R, Paracha N, Parker C, Acaster S, Bachert C, Bousquet J, et al. Episode pattern and healthcare utilisation in patients with seasonal allergic rhinitis. Allergy. 2012;67:A885.
Marple BF, Fornadley JA, Patel AA, Fineman SM, Fromer L, Krouse JH, et al. Keys to successful management of patients with allergic rhinitis: focus on patient confidence, compliance, and satisfaction. Otolaryngol Head Neck Surg. 2007;136:S107–24.
Bousquet PJ, Bachert C, Canonica GW, Casale TB, Mullol J, Klossek JM, et al. Uncontrolled allergic rhinitis during treatment and its impact on quality of life: a cluster randomized trial. J Allergy Clin Immunol. 2010;126:666–8.
Bousquet PJ, Demoly P, Devillier P, Mesbah K, Bousquet J. Impact of allergic rhinitis symptoms on quality of life in primary care. Int Arch Allergy Immunol. 2013;160:393–400.
Price D, Bousquet J, Pitman R, Lieberman P, Munzel U, Meltzer E. Sub-optimal control of allergic rhinitis: the need for a new and more effective treatment option. Allergy. 2013;68:A405.
Brozek JL, Bousquet J, Baena-Cagnani CE, Bonini S, Canonica GW, Casale TB, et al. Allergic Rhinitis and its Impact on Asthma (ARIA) guidelines: 2010 revision. J Allergy Clin Immunol. 2010;126:466–76.
Anolik R. Mometasone Furoate Nasal Spray With Loratadine Study Group. Clinical benefits of combination treatment with mometasone furoate nasal spray and loratadine vs monotherapy with mometasone furoate in the treatment of seasonal allergic rhinitis. Ann Allergy Asthma Immunol. 2008;100:264–71.
Esteitie R, deTineo M, Naclerio RM, Baroody FM. Effect of the addition of montelukast to fluticasone propionate for the treatment of perennial allergic rhinitis. Ann Allergy Asthma Immunol. 2010;105:155–61.
Bousquet J, Khaltaev N, Cruz AA, Denburg J, Fokkens WJ, Togias A, et al. Allergic Rhinitis and its Impact on Asthma (ARIA) 2008 update (in collaboration with the World Health Organization, GA(2)LEN and AllerGen). Allergy. 2008;63 Suppl 86:8–160.
Wallace DV, Dykewicz MS, Bernstein DI, Blessing-Moore J, Cox L, Khan DA, et al. The diagnosis and management of rhinitis: an updated practice parameter. J Allergy Clin Immunol. 2008;122:S1–84.
Scadding GK, Durham SR, Mirakian R, Jones NS, Leech SC, Farooque S, et al. BSACI guidelines for the management of allergic and non-allergic rhinitis. Clin Exp Allergy. 2008;38:19–42.
Dymista summary of product characteristics. 2014. https://www.medicines.org.uk/emc/medicine/27579/SPC/Dymista+Nasal+Spray/. Accessed 9 Feb 2015.
Derendorf H, Munzel U, Petzold U, Maus J, Mascher H, Hermann R, et al. Bioavailability and disposition of azelastine and fluticasone propionate when delivered by MP29-02, a novel aqueous nasal spray. Br J Clin Pharmacol. 2012;74:125–33.
Meltzer EO, LaForce C, Ratner P, Price D, Ginsberg D, Carr W. MP29-02 (a novel intranasal formulation of azelastine hydrochloride and fluticasone propionate) in the treatment of seasonal allergic rhinitis: a randomized, double-blind, placebo-controlled trial of efficacy and safety. Allergy Asthma Proc. 2012;33:324–32.
Meltzer E, Ratner P, Bachert C, Carr W, Berger W, Canonica GW, et al. Clinically relevant effect of a new intranasal therapy (MP29-02) in allergic rhinitis assessed by responder analysis. Int Arch Allergy Immunol. 2013;161:369–77.
Carr W, Bernstein J, Lieberman P, Meltzer E, Bachert C, Price D, et al. A novel intranasal therapy of azelastine with fluticasone for the treatment of allergic rhinitis. J Allergy Clin Immunol. 2012;129:1282–9.
Price D, Shah S, Bhatia S, Bachert C, Berger W, Bousquet J, et al. A new therapy (MP29-02) is effective for the long-term treatment of chronic rhinitis. J Investig Allergol Clin Immunol. 2013;23:495–503.
Berger WE, Shah S, Lieberman P, Hadley J, Price D, Munzel U, et al. Long-term, randomized safety study of MP29-02 (a novel intranasal formulation of azelastine hydrochloride and fluticasone propionate in an advanced delivery system) in subjects with chronic rhinitis. J Allergy Clin Immunol Pract. 2014;2:179–85.
Stull DE, Roberts L, Frank L, Heithoff K. Relationship of nasal congestion with sleep, mood, and productivity. Curr Med Res Opin. 2007;23:811–9.
Ciprandi G, Incorvaia C, Scurati S, Puccinelli P, Soffia S, Frati F, et al. Patient-related factors in rhinitis and asthma: the satisfaction with allergy treatment survey. Curr Med Res Opin. 2011;27:1005–11.
EMA guideline. Guideline on the clinical development of medicinal products for the treatment of allergic rhinoconjunctivitis. 2004. http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500003554.pdf. Accessed 9 Feb 2015.
Klimek L, Bachert C, Mosges R, Munzel U, Price D, Virchow JC, et al. Effectiveness of MP29-02 for the treatment of allergic rhinitis in the real life: results from a non-interventional study. Allergy Asthma Proc. 2015;36:40–7.
Bousquet J, Addis A, Adcock I, Agache I, Agusti A, Alonso A, et al. Integrated care pathways for airway diseases (AIRWAYS-ICPs). Eur Respir J. 2014;44:304–23.
We thank Dr Ruth B Murray (Medical & Scientific Affairs Consultant, Ireland) for critically reviewing this article.
GWC and OR have been consultants and speakers for MEDA in the last five years. The other authors declare that they have no competing interest concerning this present paper.
OR and GWC concepted this Editorial, contributed to acquisition, analysis and interpretation of the litereture data, and were involved in drafting the manuscript and revising it critically. IM, MC, CQ, EH and FF contributed in interepreting the litereture data, drafting the manuscript and revising it critically. All the authors gave their final approval of the submitted version of the manuscript.
GWC is the current President of the Italian Society of Allergy, Asthma and Clinical Immunology (SIAAIC).
OR is the current Treasurer of the Italian Society of Allergy, Asthma and Clinical Immunology (SIAAIC).
EH is the current Secretary General of the Italian Society of Allergy, Asthma and Clinical Immunology (SIAAIC).
IM and MC are the current Junior Members Chairpersons of the Italian Society of Allergy, Asthma and Clinical Immunology (SIAAIC).
CQ is currently member of the Junior Members Working Group of the Italian Society of Allergy, Asthma and Clinical Immunology (SIAAIC).
Ilaria Massaro, Marco Caminati, Cristina Quecchia, Filippo Fassio, Enrico Heffler and Giorgio Walter Canonica contributed equally to this work.
About this article
Cite this article
Rossi, O., Massaro, I., Caminati, M. et al. Escaping the trap of allergic rhinitis. Clin Mol Allergy 13, 17 (2015). https://doi.org/10.1186/s12948-015-0023-y
- Allergic rhinitis
- Intranasal corticosteroids
- Intranasal antihistamines