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市場調査レポート
商品コード
1378365
ユルトミリス(ULTOMIRIS)の新興薬剤に関する洞察と市場予測:2032年ULTOMIRIS Emerging Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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ユルトミリス(ULTOMIRIS)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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ユルトミリス(ラブリズマブ)は、最初で唯一の長時間作用型C5補体阻害薬であり、即効性、完全性、持続性の補体阻害作用を有します。この薬剤は、身体の免疫システムの一部である終末補体カスケードのC5タンパク質を阻害することで作用します。補体カスケードは、制御されずに活性化すると過剰に反応し、健康な細胞を攻撃します。ユルトミリスは、成人患者に8週間ごとに静脈内投与されます。
今後数年間で、皮膚筋炎の市場シナリオは、世界中の広範な調査と増加するヘルスケア支出のために変化します。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、ユルトミリス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。他の皮膚筋炎治療薬もユルトミリス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予測されています。
当レポートでは、主要7ヶ国におけるユルトミリス市場について調査し、市場の概要とともに、2024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。
“"ULTOMIRIS Emerging Drug Insight and Market Forecast - 2032" ” report provides comprehensive insights about ULTOMIRIS for dermatomyositis in the seven major markets. A detailed picture of the ULTOMIRIS for dermatomyositis 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 ULTOMIRIS for dermatomyositis. 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 ULTOMIRIS market forecast analysis for dermatomyositis in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in dermatomyositis.
ULTOMIRIS (ravulizumab), the first and only long-acting C5 complement inhibitor, offers immediate, complete, and sustained complement inhibition. The medication works by inhibiting the C5 protein in the terminal complement cascade, a part of the body's immune system. When activated uncontrolled, the complement cascade over-responds, leading the body to attack its healthy cells. ULTOMIRIS is administered intravenously every 8 weeks in adult patients, following a loading dose.
The company is actively recruiting for its registration Phase II/III study, which started in December 2021 and is expected to be completed by November 2024.
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 ULTOMIRIS for dermatomyositis 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 ULTOMIRIS for dermatomyositis covering trial interventions, trial conditions, trial status, start and completion dates.