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市場調査レポート
商品コード
1614776
APP13007市場:市場規模、予測、新たな洞察-2032年APP13007 Market Size, Forecast, and Emerging Insight - 2032 |
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カスタマイズ可能
適宜更新あり
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APP13007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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APP13007(クロベタゾールプロピオン酸エステル点眼用ナノ懸濁液)は、コルチコステロイドであるクロベタゾールプロピオン酸エステルをナノミリングし、賦形剤の混合物とともに多剤保存水性製剤に分散させた点眼用ナノ懸濁液です。独自のナノミリング技術により、プロピオン酸クロベタゾールを水性懸濁液として製剤化することができます。APP13007におけるプロピオン酸クロベタゾールナノ粒子のこの懸濁液は、眼表面への点眼時にプロピオン酸クロベタゾールの眼内への効率的な浸透を可能にし、治療上適切な濃度のプロピオン酸クロベタゾールを眼内の標的組織に送達するように設計されています。APP13007は、眼科手術後の炎症および疼痛の治療薬として開発されています。
Activusは当初、特許を取得した独自のAPNT(Activus Pure Nanoparticle Technology)を副腎皮質ステロイドであるプロピオン酸クロベタゾールに適用し、眼の術後炎症を治療するための新規ナノ粒子製剤を創製することでAPP13007を開発しました。Activusは2017年8月にFormosaに売却されました。売却後、FormosaはAPP13007の開発を進めています。
今後数年間で、世界中の広範な調査と医療支出の増加により、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、APP13007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。術後疼痛に対する他の新興製品は、APP13007に厳しい市場競争をもたらすと予想され、近い将来、後発の新興治療薬が発売されれば、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APP13007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。
"APP13007 Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about APP13007 for Postoperative pain in the seven major markets. A detailed picture of the APP13007 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 APP13007 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 APP13007 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.
APP13007 (clobetasol propionate ophthalmic nanosuspension) is an ophthalmic nanosuspension prepared by dispersing nanomilled clobetasol propionate, a corticosteroid, with a mixture of excipients in a multi-dose preserved aqueous formulation. The proprietary nanomilling technology allows clobetasol propionate to be formulated as an aqueous suspension. This suspension of clobetasol propionate nanoparticles in APP13007 is designed to enable efficient penetration of clobetasol propionate into the eye upon ocular surface instillation and deliver therapeutically relevant concentrations of clobetasol propionate to the target tissues within the eye. APP13007 is being developed for the treatment of postoperative inflammation and pain following ocular surgery.
Activus originally developed APP13007 by applying its patented proprietary APNT (Activus Pure Nanoparticle Technology) to the corticosteroid clobetasol propionate to create a novel nanoparticle formulation for treating postoperative inflammation of the eye. Activus was divested in August 2017 to Formosa. Since the divestment, Formosa has progressed in the development of APP13007.
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.
APP13007 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of APP13007 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 APP13007 for Postoperative pain covering trial interventions, trial conditions, trial status, start and completion dates.