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市場調査レポート
商品コード
1462272
バトクリマブ市場:市場規模、予測、新たな洞察- 2032年Batoclimab Market Size, Forecast, and Emerging Insight - 2032 |
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カスタマイズ可能
適宜更新あり
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バトクリマブ市場:市場規模、予測、新たな洞察- 2032年 |
出版日: 2024年04月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 2~10営業日
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Immunovantの最初の治験薬であるバトクリマブ(IMVT-1401)は、新生児Fc受容体(FcRn)を標的とする新規の完全ヒト型モノクローナル抗体です。非臨床試験および臨床試験において、バトクリマブはIgG抗体レベルを低下させることが確認されています。高濃度の病原性IgG抗体は様々な自己免疫疾患の原動力であり、その結果、この製品候補は自己皮下注射剤として様々なIgGを介する自己免疫疾患に対処できる可能性があります。
新生児Fcレセプター(FcRn)は、IgG抗体と結合し、その細胞内輸送を誘導する細胞レセプターです。FcRnはIgG抗体の分解を防ぐ上で極めて重要な役割を果たしています。したがって、FcRnを標的とする抗体でFcRnを阻害すると、病原性IgG抗体のレベルが低下することが示されています。IgGを介する自己免疫疾患における他の抗FcRn抗体の臨床試験が完了し、有望な結果が得られていることから、FcRnはこれらの関連する病態を治療するための治療上重要な医薬ターゲットであることが示唆されています。
今後数年間で、バセドウ病眼症の市場シナリオは、世界中の広範な調査と医療支出の増加により変化します。各社は、病態を治療/改善するための新たなアプローチに焦点を当てた治療法を開発し、課題を評価し、バトクリマブの優位性に影響を与える可能性のある機会を模索しています。バセドウ病眼症に対する他の新興製品がバトクリマブとの厳しい市場競争をもたらすと予想され、近い将来、後発の新興治療薬が発売されれば、市場に大きな影響を与えるとみられています。
当レポートでは、主要7ヶ国におけるバセドウ病眼症治療薬のXADAGO市場について調査し、市場の概要とともに、競合情勢、2032年までの市場規模予測、および国別市場分析などを提供しています。
"Batoclimab Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about batoclimab for Graves' Ophthalmopathy in the seven major markets. A detailed picture of the batoclimab for Graves' Ophthalmopathy 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 batoclimab for Graves' Ophthalmopathy. 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 batoclimab market forecast analysis for Graves' Ophthalmopathy in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Graves' Ophthalmopathy.
Immunovant's first investigational product, batoclimab (IMVT-1401), is a novel, fully human monoclonal antibody targeting the neonatal Fc receptor (FcRn). In nonclinical studies and clinical trials, batoclimab has been observed to reduce IgG antibody levels. High levels of pathogenic IgG antibodies drive a variety of autoimmune diseases, and, as a result, this product candidate has the potential to address a variety of IgG-mediated autoimmune diseases as a self-administered subcutaneous injection.
The neonatal Fc receptor (FcRn) is a cellular receptor that binds IgG antibodies and guides their transport through cells. FcRn plays a pivotal role in preventing the degradation of IgG antibodies. Therefore, inhibition of FcRn with an FcRn targeting antibody has been shown to reduce levels of pathogenic IgG antibodies. Completed clinical trials of other anti-FcRn antibodies in IgG-mediated autoimmune diseases have generated promising results, suggesting that FcRn is a therapeutically important pharmaceutical target to treat these relevant pathogenic conditions.
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.
Batoclimab Analytical Perspective by DelveInsight
This report provides a detailed market assessment of batoclimab for Graves' Ophthalmopathy 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 2025 to 2032.
The report provides the clinical trials information of batoclimab for Graves' Ophthalmopathy covering trial interventions, trial conditions, trial status, start and completion dates.