PUBLISHER: DelveInsight | PRODUCT CODE: 1609443
PUBLISHER: DelveInsight | PRODUCT CODE: 1609443
"SPIRIVA RESPIMAT Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about SPIRIVA RESPIMAT for Asthma in the seven major markets. A detailed picture of the SPIRIVA RESPIMAT 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 SPIRIVA RESPIMAT 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 SPIRIVA RESPIMAT market forecast analysis for Asthma in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Asthma.
SPIRIVA RESPIMAT (tiotropium bromide) is indicated to reduce exacerbations in COPD patients. SPIRIVA RESPIMAT is a bronchodilator used to treat moderate to severe persistent asthma in people 6 years of age and older whose asthma symptoms are not well controlled with asthma medicines called inhaled corticosteroids. A skin or blood test is performed to see if someone has allergies to year-round allergens.
The recommended dosage for patients with asthma is two inhalations of SPIRIVA RESPIMAT 1.25 mcg per actuation once daily; the total dose equals 2.5 mcg of SPIRIVA RESPIMAT. In treating asthma, the maximum benefits in lung function may take up to 4-8 weeks of dosing.
Tiotropium is a long-acting, antimuscarinic agent often referred to as an anticholinergic. It has similar affinity to the subtypes of muscarinic receptors, M1 to M5. In the airways, it exhibits pharmacological effects by inhibiting M3-receptors at the smooth muscle leading to bronchodilation. In preclinical in vitro and in vivo studies, prevention of methacholine-induced bronchoconstriction effects was dose-dependent and lasted longer than 24 h. The bronchodilation following inhalation of tiotropium is predominantly a site-specific effect.
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.
SPIRIVA RESPIMAT Analytical Perspective by DelveInsight
This report provides a detailed market assessment of SPIRIVA RESPIMAT 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 SPIRIVA RESPIMAT for Asthma covering trial interventions, trial conditions, trial status, start and completion dates.