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시장보고서
상품코드
1462289
DPX-Survivac 시장 규모, 예측, 신약 인사이트(2032년)DPX-Survivac Market Size, Forecast, and Emerging Insight - 2032 |
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Immunvaccine이 개발중인 Maveropepimut-S(MVP-S, 구 DPX-Survivac)는 DPX 플랫폼과 암 항원 서바이빈(Survivin)을 결합한 T세포 활성화 면역요법입니다. 생체 내에서 표적 T세포를 생성하는 IMV의 새로운 면역치료제 계열의 선도적 임상 후보물질입니다. DPX-Survivac은 Merck KGaA로부터 전 세계 독점 라이선스를 획득한 서바이빈 기반 항원(Survivin-based antigen)을 사용하여 Depo-Proteins를 사용하며, DepoVax 백신 전달 플랫폼으로 제형화됩니다.
현재 플래티넘 제제 내성 상피성 난소암을 대상으로 한 임상 2상(AVALON)이 진행 중이며, 2025년 8월까지 완료될 예정입니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 난소암용 DPX-Survivac에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"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.