DelveInsight’s “Allergic Rhinitis Market Insights, Epidemiology, and Market Forecast – 2034” report delivers an in-depth understanding, historical and forecasted epidemiology, as well as the Allergic Rhinitis market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.
The Allergic Rhinitis Market is an evolving segment of the global healthcare landscape, driven by the increasing Allergic Rhinitis prevalence of the disorder and the continuous development of innovative treatment options. The Allergic Rhinitis Market encompasses various therapeutic categories, including antipsychotics, adjunctive therapies, and emerging treatment modalities.
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Key Takeaways from the Allergic Rhinitis Market Report
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Allergic rhinitis Epidemiology Segmentation in the 7MM
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Allergic rhinitis Marketed Drugs
RYALTRIS is a metered, fixed-dose, aqueous suspension, prescription drug product nasal spray approved by the FDA for treating symptoms associated with Seasonal Allergic Rhinitis. Each unit of Ryaltris nasal spray contains 665 mcg of olopatadine hydrochloride, a histamine-1(H1)-receptor inhibitor, and 25 mcg of mometasone furoate, a corticosteroid. In January 2022, RYALTRIS was approved by the US FDA for treating symptoms associated with seasonal allergic rhinitis in adults and pediatric patients 12 years of age and older. In August 2021, Glenmark Pharmaceuticals received marketing approval for its fixed-dose combination nasal spray RYALTRIS in 13 countries across the European Union and the UK.
Allergic Rhinitis Emerging Drugs
REGN5713-5714-5715 is an investigational combination of three fully human monoclonal antibodies designed to treat allergic inflammatory conditions caused by the allergen Betv1, which is the main allergen responsible for birch pollen allergies. Birch allergy can trigger reactions such as allergic rhinitis and asthma. The Bet v1-specific mAbs (REGN5713, REGN5714, and REGN5715) were generated using Regeneron’s VelocImmune platform. Preclinical studies demonstrated that the three mAbs bind independently and non-competitively to Bet v 1. All three together provided maximal inhibition of Bet v 1 binding to human polyclonal IgE and potently blocked basophil activation ex vivo and mast cell degranulation in vivo. The multi-antibody therapy is currently in Phase III of development.
Grass MATA MPL contains an extract of 13 grass pollens modified with glutaraldehyde to form allergoids that reduce the reactivity with immunoglobulin E (IgE) antibodies without a reduction in other important immunological properties, such as T-cell reactivity. The allergoid is adsorbed to microcrystalline tyrosine as a depot adjuvant system formulation. Monophosphoryl lipid-A (MPL) is included as an adjuvant to increase the immunogenic effect of the immunotherapy and to enhance the switch from an allergen-specific helper T-cell Type 2 (Th2) to helper T-cell Type 1 (Th1) like an immune response. Grass MATA MPL is being developed as a pre-seasonal SC immunotherapy product for treating allergic rhinitis and/or rhinoconjunctivitis. In November 2023, Allergy Therapeutics completed the Phase III study to evaluate the efficacy and safety of PQ grass in subjects with seasonal allergic rhinitis and/or rhinoconjunctivitis induced by grass pollen.
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Scope of the Allergic Rhinitis Market Report
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Table of Content
1 Key Insights
2 Report Introduction
3 Allergic Rhinitis Market Overview at a Glance
4 Epidemiology and Market Forecast Methodology
5 Key Events
6 Executive Summary of of Allergic rhinitis
7 Disease Background and Overview of Allergic Rhinitis
8 Epidemiology and Patient Population of Allergic Rhinitis
9 Patient Journey
10 Marketed Drugs
11 Emerging Drugs
12 Allergic Rhinitis: Seven Major Market Analysis
13 Key Opinion Leaders’ Views
14 SWOT Analysis
15 Unmet needs
16 Market Access and Reimbursement
17 Appendix
18 DelveInsight Capabilities
19 Disclaimer
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