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市場調査レポート
商品コード
1381114
AV-GBM-1の新興薬剤に関する洞察と市場予測:2032年AV-GBM-1 Emerging Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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AV-GBM-1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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AV-GBM-1は、培養した自己多形性膠芽腫(GBM)腫瘍細胞由来の自己複製腫瘍開始細胞に由来する自己腫瘍抗原を担持した自己樹状細胞からなる新規免疫療法であり、免疫賦活作用および抗腫瘍作用が期待されます。本治療法は、補助療法として一連のSC注射で投与されます。この治療薬はユニークな汎抗原性で、疾患の急速な増殖と標準治療に対する抵抗性の原因である自己腫瘍開始細胞上の複数の抗原を標的とします。AV-GBM-1を投与すると、自己のTAA担持DCが免疫系をGBM新抗原に暴露し、その結果、自己のGBM細胞に対する細胞傷害性Tリンパ球(CTL)媒介免疫応答が起こり、GBM細胞が溶解します。
Aivita Biomedicalは、AV-GBM-1を新たに診断されたGBMに対する潜在的治療薬として、第III相臨床試験で検討しています。
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、AV-GBM-1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-1を対象とする他の新興製品はAV-GBM-1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AV-GBM-1市場について調査し、市場の概要とともに、2027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。
“"AV-GBM-1 Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about AV-GBM-1 for glioblastoma multiforme (GBM) in the seven major markets. A detailed picture of the AV-GBM-1 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 AV-GBM-1 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 AV-GBM-1 market forecast analysis for GBM in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in GBM.
AV-GBM-1 is novel immunotherapy consisting of autologous dendritic cells loaded with autologous tumor antigens derived from self-renewing tumor-initiating cells derived from cultured autologous glioblastoma multiforme (GBM) tumor cells, with potential immunostimulatory and antineoplastic activities. The treatment is administered in a series of SC injections as adjunctive therapy. It is uniquely pan-antigenic, targeting multiple antigens on autologous tumor-initiating cells responsible for the rapid growth of the disease and resistance to standard therapy. Upon administration, the autologous TAA-loaded DCs AV-GBM-1 expose the immune system to the GBM neoantigens, which results in a cytotoxic T-lymphocyte (CTL)-mediated immune response against the autologous GBM cells leading to GBM cell lysis.
Aivita Biomedical investigates AV-GBM-1 as a potential treatment for newly diagnosed GBM in Phase III clinical trial.
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 AV-GBM-1 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 2027 to 2032.
The report provides the clinical trials information of AV-GBM-1 for GBM covering trial interventions, trial conditions, trial status, start and completion dates.