市場調査レポート
商品コード
1462309
OZAWADE市場:市場規模、予測、市場洞察-2032年OZAWADE Market Size, Forecast, and Market Insight - 2032 |
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OZAWADE市場:市場規模、予測、市場洞察-2032年 |
出版日: 受注後更新
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 2~10営業日
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OZAWADEは、CPAPなどの一次的なOSA治療で十分な眠気が得られない成人OSA患者、またはこの治療に耐えられない患者において、覚醒度の改善とEDSの軽減を適応とします。本治療は、OSAおよび心血管リスクを専門とする医師によって開始されなければならず、OSAは毎年再評価されなければなりません。OZAWADEはOSA患者の気道閉塞の治療薬ではありません。OSAの一次治療は維持されるか、一次治療に耐えられない患者では定期的に再提案されなければなりません。
2023年1月、アキュリス製薬は、OSAを伴うEDS患者を対象としたピトリサントの第Ⅲ相臨床試験を日本で開始しました。
今後数年間で、閉塞性睡眠時無呼吸症候群(OSA)の市場シナリオは、世界中の広範な調査と医療支出の増加により変化します。各社は、病状を治療/改善するための新たなアプローチに焦点を当てた治療法を開発し、課題を評価し、OZAWADEの優位性に影響を与える可能性のある機会を模索しています。他のOSA治療薬もOZAWADEと厳しい市場競争を繰り広げることが予想され、近い将来、後発の新興治療薬が上市されれば、市場に大きな影響を与えるとみられています。
当レポートでは、主要6ヶ国における閉塞性睡眠時無呼吸症候群(OSA)治療薬のOZAWADE市場について調査し、市場の概要とともに、競合情勢、2032年までの市場規模予測、および国別市場分析などを提供しています。
"OZAWADE Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about OZAWADE for Obstructive sleep apnea (OSA) in the six major markets. A detailed picture of the OZAWADE for OSA in the 6MM, i.e., 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 OZAWADE for OSA. 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 OZAWADE market forecast analysis for OSA in the 6MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in OSA.
OZAWADE is indicated to improve wakefulness and reduce EDS in adult patients with OSA whose sleepiness is not satisfactorily addressed by primary OSA treatment such as CPAP or those who do not tolerate this treatment. The treatment must be initiated by a physician specializing in OSA and cardiovascular risks; OSA must be re-assessed annually. OZAWADE is not a treatment for airway obstruction in patients with OSA. The primary treatment of OSA must be maintained or regularly re-proposed in patients who have not tolerated the primary treatment.
In January 2023, Aculys Pharma initiated a Phase III trial of Pitolisant treating patients with EDS associated with OSA in Japan.
Dosage
OZAWADE should be used at the lowest effective dose based on clinical response and patient tolerance. The optimal therapeutic dose must be reached in stages, without exceeding the dose of 18 mg/day:
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.
OZAWADE Analytical Perspective by DelveInsight
This report provides a detailed market assessment of OZAWADE for Obstructive sleep apnea (OSA) in the six major markets, i.e., 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 OZAWADE for OSA covering trial interventions, trial conditions, trial status, start and completion dates.