市場調査レポート
商品コード
1462308
OSE-2101の市場規模、予測、新薬の考察(2032年)OSE-2101 Market Size, Forecast, and Emerging Insight - 2032 |
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OSE-2101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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OSE-2101(Tedopi)は、OSE Immunotherapeuticの最先端製品であり、治療用ネオエピトープ系ワクチンで、T細胞を特異的に活性化する5つの腫瘍抗原から選択され最適化された9つのネオエピトープと、T細胞の活性化を標的とした万能ヘルパーT細胞応答を与える1つのエピトープを独自に組み合わせたものです。Tedopiは、細胞傷害性応答の重要な受容体であるHLA-A2+患者向けに設計された治療薬です。
現在、Tedopiは3群からなるTEDOVAフェーズII試験で検討されており、腫瘍学協同グループARCAGY-GINECOの支援のもと、プラチナ製剤感受性再発卵巣がん患者を対象に、プラチナ製剤ベースの化学療法後に病勢がコントロールされた場合の維持療法として、単独または抗PD-1薬キイトルーダとの併用で、最良の支持療法と比較評価されています。
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OSE-2101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。
"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.