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市場調査レポート
商品コード
1377991
MTG201+ニボルマブの新興薬剤に関する洞察と市場予測:2032年MTG201 + nivolumab Emerging Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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MTG201+ニボルマブの新興薬剤に関する洞察と市場予測:2032年 |
出版日: 2023年11月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 1~3営業日
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MTG201は、様々ながんに対応可能な独自の二重作用機序を有する新規の治験用遺伝子治療薬です。本薬候補は、当社独自のアデノウイルスベクター技術プラットフォームを活用し、不死化細胞/Dickkopf-3遺伝子(REIC/Dkk-3遺伝子)の発現が著しく低下しているがん細胞に、発現低下したREIC/Dkk-3遺伝子を導入します。その結果、がん細胞におけるREIC/Dkk-3遺伝子の発現が増加し、がん細胞で選択的に免疫原性細胞死が引き起こされます。同時に、腫瘍組織内の正常細胞成分におけるREIC/Dkk3遺伝子の発現増加は、樹状細胞とナチュラルキラー(NK)細胞を活性化することによって抗腫瘍免疫を促進する一方で、免疫抑制性の制御性T細胞(Treg)と骨髄由来抑制細胞(MDSC)を抑制します。このような新規の二重メカニズムに基づき、MTG201はニボルマブのようなチェックポイント阻害薬との相乗効果が期待できると考えられています。
テキサス州ヒューストンのベイラー医科大学で実施された第II相試験(NCT04013334)は、ニボルマブとの併用によるMTG201の腫瘍内投与の有効性、安全性、忍容性を評価するためにデザインされた非盲検単群試験です。本試験では、プラチンベースの全身化学療法が無効となった悪性中皮腫患者を最大12人まで登録しました。本試験の主要目的は併用療法の有効性を評価することであり、主要評価項目は客観的奏効率(ORR)です。
当レポートでは、主要7ヶ国におけるMTG201+ニボルマブ市場について調査し、市場の概要とともに、2024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。
“"MTG201 + nivolumab Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about MTG201 + nivolumab for malignant pleural mesothelioma (MPM) in the seven major markets. A detailed picture of the MTG201 + nivolumab for MPM 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 MTG201 + nivolumab for MPM. 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 MTG201 + nivolumab market forecast analysis for MPM in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in MPM.
MTG201 is novel investigational gene therapy with unique dual mechanisms of action capable of addressing a range of cancers. The drug candidate leverages the company's proprietary adenoviral vector technology platform to deliver the reduced expression in immortalized Cells/Dickkopf-3 gene (REIC/Dkk-3 gene) into cancer cells, where the expression of the gene is markedly downregulated. The resulting increase in REIC/Dkk-3 gene expression in cancer cells triggers immunogenic cell death selectively in cancer cells. At the same time, increased expression of the REIC/Dkk3 gene in normal cell components in tumor tissue promotes antitumor immunity by activating dendritic cells and natural killer (NK) cells while suppressing immune-suppressive regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSC). Based on these novel dual mechanisms, MTG201 is believed to be well-positioned to work synergistically with checkpoint inhibitors such as nivolumab.
The Phase II trial (NCT04013334), conducted at the Baylor College of Medicine in Houston, Texas, is an open-label, single-arm study designed to assess the efficacy, safety, and tolerability of intratumoral administration of MTG201 in combination with nivolumab. The trial enrolled up to twelve patients with malignant mesothelioma who have failed front-line systemic platin-based chemotherapy. The study's primary objective is to assess the efficacy of the treatment combination, with the primary endpoint being objective response rate (ORR).
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.
MTG201 + nivolumab Analytical Perspective by DelveInsight
This report provides a detailed market assessment of MTG201 + nivolumab for malignant pleural mesothelioma (MPM) 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 2024 to 2032.
The report provides the clinical trials information of MTG201 + nivolumab for MPM covering trial interventions, trial conditions, trial status, start and completion dates.
Key Questions