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시장보고서
상품코드
1462308
OSE-2101 시장 규모, 예측, 신약 인사이트(2032년)OSE-2101 Market Size, Forecast, and Emerging Insight - 2032 |
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OSE-2101(Tedopi)은 OSE Immunotherapeutic의 최첨단 제품인 치료용 네오에피토프 기반 백신으로, T세포를 특이적으로 활성화하는 5가지 종양 항원으로부터 선별되고 최적화된 9개의 네오에피토프와 T세포 활성화를 표적으로 하는 만능 T세포 반응을 제공하는 하나의 헬퍼 T세포 반응을 유도하는 하나의 에피토프(epitope)를 독자적으로 조합한 테도피는 세포독성 반응의 중요한 수용체인 HLA-A2 환자를 위해 설계된 치료제입니다.
현재 테도피는 종양학 협력단체인 ARCAGY-GINECO의 지원을 받아 백금 민감성 재발성 난소암 환자를 대상으로 백금 기반 화학요법 후 질병이 조절된 경우, 유지요법으로 단독 또는 항 PD-1제제 키트루다와 병용하여 최선의 지지요법으로 평가하기 위해 3군으로 구성된 TEDOVA 임상 2상 시험이 진행 중입니다. 으로 단독 또는 항 PD-1 치료제 키트루다와 병용하여 최선의 지지요법과 비교 평가되고 있습니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 난소암용 OSE-2101에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"OSE-2101 Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about OSE-2101 for ovarian cancer in the seven major markets. A detailed picture of the OSE-2101 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 OSE-2101 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 OSE-2101 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.
OSE-2101 (Tedopi) - OSE Immunotherapeutic's most advanced product and therapeutic neo-epitope-based vaccine - is a proprietary combination of nine optimized neo-epitopes, selected and optimized from five tumoral antigens to activate specifically T cells, plus one epitope giving universal helper T cell response targeting T cell activation. It is a treatment designed for HLA-A2+ patients, a key receptor of the cytotoxic response.
Currently, Tedopi is being studied in a three-arm TEDOVA Phase II study, which is evaluating it as a maintenance treatment, alone or in combination with the anti-PD-1 KEYTRUDA, versus the best supportive care in platinum-sensitive recurrent ovarian cancer patients, with the controlled disease after platinum-based chemotherapy under the sponsorship of cooperative group in oncology ARCAGY-GINECO.
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.
OSE-2101 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of OSE-2101 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 OSE-2101 for ovarian cancer covering trial interventions, trial conditions, trial status, start and completion dates.