市場調査レポート
商品コード
1462289
DPX-Survivacの市場規模、予測、新薬の考察( 2032年)DPX-Survivac Market Size, Forecast, and Emerging Insight - 2032 |
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DPX-Survivacの市場規模、予測、新薬の考察( 2032年) |
出版日: 受注後更新
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 2~10営業日
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Immunvaccineが開発中のMaveropepimut-S(MVP-S、旧称DPX-Survivac)は、DPXプラットフォームとがん抗原サバイビンを組み合わせたT細胞活性化免疫療法です。これは、生体内で標的T細胞を生成するIMVの新しいクラスの免疫療法のリード臨床候補です。サバイビン特異的キラーT細胞を活性化することにより、Maveropepimut-Sはがん細胞の破壊を促進し、がん細胞の生成と生存の基本的プロセスを破壊します。DPX-Survivacは、Merck KGaAから全世界独占的にライセンスされたサバイビンベースの抗原を使用し、DepoVaxワクチンデリバリープラットフォームで製剤されます。
現在、プラチナ製剤抵抗性上皮性卵巣がんを対象としたフェーズII臨床試験(AVALON)が実施されており、2025年8月までに完了する見込みです。
当レポートでは、主要7市場(米国・ドイツ・フランス・イタリア・スペイン・英国・日本)における卵巣がん向けDPX-Survivacについて調査分析し、作用機序、用法と用量、研究開発活動についての考察、収益の予測などを提供しています。
"DPX-Survivac Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about DPX-Survivac for ovarian cancer in the seven major markets. A detailed picture of the DPX-Survivac for ovarian cancer 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 DPX-Survivac for ovarian cancer. 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 DPX-Survivac market forecast analysis for ovarian cancer in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in ovarian cancer.
Maveropepimut-S (MVP-S, previously known as DPX-Survivac), being developed by Immunvaccine, is a T cell activating immunotherapy that combines the power of DPX Platform with cancer antigen survivin. It is the lead clinical candidate in IMV's new class of immunotherapies that generates targeted T cells in vivo. By activating survivin-specific killer T cells, maveropepimut-S promotes the destruction of cancer cells and disrupts the fundamental processes of cancer cell production and survival. DPX-Survivac uses Survivin-based antigens in-licensed from Merck KGaA on a worldwide exclusive basis and formulated in the DepoVax vaccine delivery platform.
It is currently being investigated in Phase II clinical trial (AVALON) for the potential treatment of platinum-resistant epithelial ovarian cancer that is estimated to be completed by August 2025.
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.
DPX-Survivac Analytical Perspective by DelveInsight
This report provides a detailed market assessment of DPX-Survivac for ovarian cancer 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 DPX-Survivac for ovarian cancer covering trial interventions, trial conditions, trial status, start and completion dates.