|
시장보고서
상품코드
1609440
AIRSUPRA 시장 규모, 예측, 시장 인사이트(2032년)AIRSUPRA Market Size, Forecast, and Market Insight - 2032 |
||||||
FDA는 18세 이상 천식 환자의 기관지 수축 치료 또는 예방, 천식 발작 위험 감소를 위해 AIRSUPRA(알부테롤, 부데소니드) 흡입용 에어로졸을 승인했으며, AIRSUPRA는 알부테롤과 부데소니드를 모두 포함하고 있습니다. 이 두 약제는 천식의 임상, 생리학 및 염증 지수에 대해 서로 다른 효과를 나타내는 두 가지 약물 계열(속효성 선택적 β2-adrenergic agonist와 합성 코르티코스테로이드)을 나타냅니다.
이 치료법은 근육을 이완시키고 폐 호흡기의 염증을 감소시켜 심각한 천식 발작의 위험을 줄여주며, 알부테롤 90mcg과 부데소니드 80mcg을 1회 2회(총 용량은 알부테롤 180mcg과 부데소니드 160mcg), 천식 증상에 따라 경구 흡입으로 투여합니다. 천식 증상에 따라 경구 흡입으로 투여합니다.
FDA는 2023년 1월에 승인했습니다.
주요 7 시장(미국, 독일, 프랑스, 이탈리아, 스페인, 영국, 일본)의 천식용 AIRSUPRA에 대해 조사분석했으며, 시장 규모 예측 및 작용기서, 용법과 용량, 연구개발 활동 등의 정보를 제공하고 있습니다.
"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.