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市場調査レポート
商品コード
1381109
DCVax-Lの新興薬剤に関する洞察と市場予測:2032年DCVax-L Emerging Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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DCVax-L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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DCVax-Lは、患者の腫瘍組織から採取された腫瘍溶解液(腫瘍細胞を処理したタンパク質抽出液)からがん抗原を用いて作られます。そのため、DCVax-Lは腫瘍抗原のフルセットを組み込んでおり、上述のように腫瘍がそれを回避する方法(「エスケープ・バリアント」)を見つけることを困難にしています。これは、GBM脳腫瘍および卵巣がんの臨床試験で使用されたDCVax製品であり、現在第III相試験中です。DCVax-Lは、標準治療の一環として患者が外科的に腫瘍を摘出する状況において、あらゆる固形がんに対して使用されることが期待されます。
今後数年間で、多形性膠芽腫(GBM)の市場シナリオは、世界中の広範な研究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、DCVax-L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。GBMを対象とした他の新興製品がDCVax-L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DCVax-L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。
“"DCVax-L Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about DCVax-L for glioblastoma multiforme (GBM) in the seven major markets. A detailed picture of the DCVax-L for GBM 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 DCVax-L for GBM. 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 DCVax-L market forecast analysis for GBM in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in GBM.
DCVax-L is made with cancer antigens from tumor lysate (a protein extract from processed tumor cells) from the patient's tumor tissue. As such, DCVax-L incorporates the full set of tumor antigens, making it difficult for tumors to find ways around it ("escape variants"), as described above. This is the DCVax product used in the GBM brain cancer and ovarian cancer clinical trials and is currently in the Phase III trial. DCVax-L is expected to be used for any solid tumor cancers in situations where the patient has their tumor surgically removed as part of standard care.
For DCVax-L, the monocytes are differentiated into dendritic cells and matured, activated, and loaded with biomarkers ("antigens") from the patient's tumor tissue (which is collected in a simple kit at the time of surgery to remove the tumor). The loading of biomarkers into the dendritic cells "educates" them about what the immune system needs to attack. The activated, educated dendritic cells are then isolated with very high purity and comprise the DCVax-L personalized vaccine. DCVax -L is administered to the patient through a simple intra-dermal injection in the upper arm, similar to a flu shot. The dendritic cells then convey the tumor biomarker information to the rest of the immune system agents (T cells, B cells, and others) as "marching orders," and the immune system agents fan out through the body, searching for anything with these biomarkers and attacking it.
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 DCVax-L for glioblastoma multiforme (GBM) 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 2023 to 2032.
The report provides the clinical trials information of DCVax-L for GBM covering trial interventions, trial conditions, trial status, start and completion dates.