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市場調査レポート
商品コード
1609440
AIRSUPRAの市場規模、予測、市場考察(2032年)AIRSUPRA Market Size, Forecast, and Market Insight - 2032 |
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カスタマイズ可能
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AIRSUPRAの市場規模、予測、市場考察(2032年) |
出版日: 2024年12月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 2~10営業日
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FDAはAIRSUPRA(アルブテロール、ブデソニド)吸入エアロゾルを、18歳以上の喘息患者における気管支収縮の治療または予防、喘息発作のリスク軽減を適応として承認しました。AIRSUPRAはアルブテロールとブデソニドの両方を含みます。これらの薬剤は、喘息の臨床、生理学、炎症指数に対し異なる効果を持つ2つの薬剤クラス(短時間作用型の選択的β2アドレナリン作動薬と合成コルチコステロイド)を示します。
この治療は、筋肉を弛緩させ、肺気道の炎症を抑えることで、重篤な喘息発作のリスクを軽減します。AIRSUPRAは、アルブテロール90mcgとブデソニド80mcgの併用を1回につき2回(総用量はアルブテロール180mcgとブデソニド160mcg)、喘息の症状に応じて経口吸入で投与します。
FDAはこれを2023年1月に承認しました。
当レポートでは、主要7市場(米国、ドイツ、フランス、イタリア、スペイン、英国、日本)における喘息向けAIRSUPRAについて調査分析し、市場規模の予測や、作用機序、用法と用量、研究開発活動などの情報を提供しています。
"AIRSUPRA Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about AIRSUPRA for Asthma in the seven major markets. A detailed picture of the AIRSUPRA for Asthma in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2019 -2032 is provided in this report along with a detailed description of the AIRSUPRA for Asthma. The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the AIRSUPRA market forecast analysis for Asthma in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Asthma.
FDA has approved AIRSUPRA (albuterol and budesonide) inhalation aerosol for the as-needed treatment or prevention of bronchoconstriction and to reduce the risk of asthma attacks in patients with asthma 18 years and older. AIRSUPRA contains both albuterol and budesonide. These drugs represent two classes of medications (a short-acting selective beta2-adrenergic agonist and a synthetic corticosteroid) that have different effects on clinical, physiological, and inflammatory indices of asthma.
The treatment works to relax the muscles and reduce inflammation in the lung airways to reduce the risk of severe asthma attacks. AIRSUPRA is given as two oral inhalations of a combination of albuterol 90 mcg and budesonide 80 mcg per inhalation (total dose albuterol 180 mcg and budesonide 160 mcg) as needed for asthma symptoms.
The FDA approved it in January 2023.
The recommended dosage of AIRSUPRA is albuterol 180 mcg and budesonide 160 mcg (administered as two actuation of AIRSUPRA [albuterol/budesonide 90 mcg/80 mcg]) as needed for asthma symptoms by oral inhalation. Do not take more than six doses (12 inhalations) in 24 h.
The report provides insights into:
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.
AIRSUPRA Analytical Perspective by DelveInsight
This report provides a detailed market assessment of AIRSUPRA for Asthma in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2024 to 2032.
The report provides the clinical trials information of AIRSUPRA for Asthma covering trial interventions, trial conditions, trial status, start and completion dates.