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市場調査レポート
商品コード
1381065
APP13007の新興薬剤に関する洞察と市場予測:2032年APP13007 Emerging Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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APP13007の新興薬剤に関する洞察と市場予測:2032年 |
出版日: 2023年11月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 1~3営業日
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APP13007は、術後の眼炎症治療薬として開発中のコルチコステロイド・クロベタゾールのナノ粒子製剤です。Activus社は当初、特許取得済みの独自技術であるActivus Pure Nanoparticle Technology(APNT)を副腎皮質ステロイド薬であるプロピオン酸クロベタゾールに応用し、眼の術後炎症治療用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。奏効率は、APP13007がフェーズIIIの重要な評価項目である炎症と疼痛の軽減において競合薬を上回ることを強く示唆しています。
APP13007は2020年に第II相試験を完了し、2021年3月に米国で第III相試験を開始しました。
2022年8月、Formosa Pharmaceuticals, Inc.とAimMax Therapeutics, Inc.は、APP13007の2つの重要な第III相臨床試験のうち、2番目の試験であるCPN-302のトップライン結果が良好であったと報告しました。
当レポートでは、主要8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、2023年~2032年の売上予測データ、競合情勢、および国別動向などを提供しています。
“"APP13007 Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about APP13007 for acute ocular pain (AOP) in the eight major markets. A detailed picture of the APP13007 for acute ocular pain in the 8MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, Canada and South Korea for the study period 2019 -2032 is provided in this report along with a detailed description of the APP13007 for acute ocular 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 acute ocular pain in the 8MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in acute ocular pain.
APP13007 is a nanoparticle formulation of the corticosteroid clobetasol in development for treating postoperative inflammation of the eye. Activus initially developed APP13007 by applying its patented proprietary Activus Pure Nanoparticle Technology (APNT) to the corticosteroid clobetasol propionate to create a novel nanoparticle formulation for treating postoperative inflammation of the eye. Response rate strongly suggests APP13007 outperforms competitors in reducing inflammation and pain for critical Phase III endpoints.
APP13007 completed Phase II studies in 2020 and started Phase III studies in the United States in March 2021.
In Aug 2022, Formosa Pharmaceuticals, Inc. and AimMax Therapeutics, Inc. (United States) reported successful top-line results from CPN-302, the second of the two pivotal Phase III clinical studies 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.
This report provides a detailed market assessment of APP13007 for acute ocular pain in the eight major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, Canada and South Korea. This segment of the report provides forecasted sales data from 2023 to 2032.
The report provides the clinical trials information of APP13007 for acute ocular pain covering trial interventions, trial conditions, trial status, start and completion dates.