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市場調査レポート
商品コード
1614774
DSUVIA市場:市場規模、予測、新たな洞察-2032年DSUVIA Market Size, Forecast, and Market Insight - 2032 |
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カスタマイズ可能
適宜更新あり
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DSUVIA市場:市場規模、予測、新たな洞察-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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DZUVEOとして知られるDSUVIAは、オピオイド作動薬であるスフェンタニルを含有しており、オピオイド鎮痛薬を必要とするほど重篤で代替治療が不十分な急性疼痛の管理のため、病院、外科センター、救急部などの認定医療監視下のヘルスケア環境における成人への使用を適応としています。
2021年1月、AcelRxは、クリーブランド大学病院メディカルセンターとの共同研究として、特殊な回復強化プロトコールに従って心肺バイパスを使用する心臓手術を受ける患者の前向きコホートにおける本剤の術後使用を評価するための医師主導治験を発表しました。2020年8月、整形外科手術の術後回復に対するDSUVIAの効果を評価するため、Cleveland Clinicとの医師主導治験が開始されました。この二重盲検試験では、膝関節鏡を受ける患者を対象に、DSUVIAとフェンタニルの静脈内投与を比較します。
今後数年間で、世界中の広範な調査と医療費の増加により、術後痛の市場シナリオは変化します。各社は、病態を治療/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、DSUVIA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。他の術後疼痛治療薬もDSUVIA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7ヶ国におけるDSUVIA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。
"DSUVIA Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about DSUVIA for Postoperative pain in the seven major markets. A detailed picture of the DSUVIA for Postoperative pain 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 DSUVIA for Postoperative pain. 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 DSUVIA market forecast analysis for Postoperative pain in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Postoperative pain.
DSUVIA, known as DZUVEO, contains sufentanil, an opioid agonist, and is indicated for use in adults in a certified medically supervised healthcare setting, such as hospitals, surgical centers, and emergency departments, for the management of acute pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate.
In January 2021, AcelRx announced an investigator-initiated study with University Hospitals Cleveland Medical Center to evaluate the postoperative use of the drug in a prospective cohort of patients undergoing cardiac surgery with cardiopulmonary bypass following a specialized enhanced recovery protocol. In August 2020, an investigator-initiated study with Cleveland Clinic was initiated to assess the effects of DSUVIA on postoperative recovery from orthopedic surgery. This double-blind study compares DSUVIA to IV fentanyl for patients undergoing knee arthroscopy.
Dosage and administration
The recommended dosage of DSUVIA is 30 mcg sublingually as needed, with a minimum of 1 h between doses; do not exceed 12 tablets in 24 h. The maximum cumulative dose is 360 mcg or 12 tablets (12 tablets X 30 mcg/dose).
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.
DSUVIA Analytical Perspective by DelveInsight
This report provides a detailed market assessment of DSUVIA for Postoperative pain 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 DSUVIA for Postoperative pain covering trial interventions, trial conditions, trial status, start and completion dates.