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市場調査レポート
商品コード
1397397
EPKINLYの薬剤に関する洞察と市場予測:2032年EPKINLY Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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EPKINLYの薬剤に関する洞察と市場予測:2032年 |
出版日: 2023年12月19日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 1~3営業日
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EPKINLY(別名エプコリタマブ、GEN3013)は、Genmab独自のDuoBody技術を用いて創製されたIgG1二重特異性抗体です。Genmab社のDuoBody-CD3技術は、細胞傷害性T細胞を選択的に誘導し、標的細胞種に対する免疫応答を誘発します。エプコリタマブは、T細胞のCD3およびB細胞のCD20に結合し、T細胞を介したCD20+細胞の殺傷を誘導するように設計されています。
エプコリタマブは、AbbVieとGenmabのがん領域における共同研究の一環として共同開発されています。両社は米国と日本における商業的責任を分担し、AbbVieはさらなる世界な商業化を担当します。両社は、エプコリタマブの単剤療法および併用療法について、さまざまな血液悪性腫瘍の治療ライン全体で評価することにコミットしています。これには、R/R DLBCL患者を対象にエプコリタマブ単剤療法を評価する進行中の第III相非盲検無作為化臨床試験や、R/R FL患者を対象にエプコリタマブ併用療法を評価する第III相非盲検臨床試験が含まれます。
当レポートでは、主要7ヶ国におけるEPKINLY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。
"EPKINLY Drug Insight and Market Forecast - 2032" report provides comprehensive insights about EPKINLY for Diffuse Large B-cell lymphoma (DLBCL) in the seven major markets. A detailed picture of the EPKINLY for DLBCL 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 EPKINLY for DLBCL. 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 EPKINLY market forecast analysis for DLBCL in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in DLBCL.
EPKINLY (also known as Epcoritamab, GEN3013) is an IgG1-bispecific antibody created using Genmab's proprietary DuoBody technology. Genmab's DuoBody-CD3 technology directs cytotoxic T cells selectively to elicit an immune response toward target cell types. Epcoritamab is designed to bind to CD3 on T cells and CD20 on B cells and induce T-cell mediated killing of CD20+ cells.
Epcoritamab is being codeveloped by AbbVie and Genmab as part of the companies' oncology collaboration. The companies will share commercial responsibilities in the US and Japan, with AbbVie responsible for further global commercialization. The companies are committed to evaluating epcoritamab as a monotherapy, and in combination, across lines of therapy in a range of hematologic malignancies. This includes an ongoing Phase III, open-label, randomized clinical trial evaluating epcoritamab as a monotherapy in patients with R/R DLBCL and a Phase III, open-label clinical trial evaluating epcoritamab in combination in patients with R/R FL.
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 EPKINLY for Diffuse Large B-cell lymphoma (DLBCL) 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 EPKINLY for DLBCL covering trial interventions, trial conditions, trial status, start and completion dates.