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市場調査レポート
商品コード
1378357
PRN-1008の新興薬剤に関する洞察と市場予測:2032年PRN-1008 Emerging Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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PRN-1008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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リルザブルチニブ(PRN-1008)は、経口投与のブルトン型チロシンキナーゼ(BTK)の可逆的共有結合阻害剤です。BTKは、B細胞受容体(BCR)、Fcガンマ受容体、Fcイプシロン受容体経路の下流に位置する必須のシグナル伝達要素です。BTKの活性化はB細胞の活性化と成熟に不可欠です。BTKはまた、Fc受容体シグナル伝達を通じて、マクロファージ、好中球、肥満細胞などのその他の免疫細胞の抗体媒介活性化も制御しています。この薬剤候補は、B細胞を枯渇させることなく、効果的かつ安全にB細胞の機能を調節できる即効性の経口治療薬であり、自己免疫疾患や炎症性疾患の治療における大きな進歩になると期待されています。
前臨床試験において、PRN1008は抗CD41誘発ITPモデルマウスにおいて、用量依存的に有意な血小板減少抑制効果を示しました。PRN1008は、抗体駆動型ラット関節炎モデルおよび自然発症の自己抗体介在性イヌ天疱瘡において、迅速かつ有意な抗炎症作用を示しました。前臨床データは、PRN1008が脾臓マクロファージにおける自己抗体/Fcガンマレセプターシグナル伝達の阻害を介して血小板破壊を減少させ、B細胞活性化における自己抗体生成効果に影響を与え、ITPにおける血小板損失を減少させる可能性を示唆しています。
当レポートでは、主要7ヶ国におけるPRN-1008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。
“"PRN-1008 Emerging Drug Insight and Market Forecast - 2032" ” report provides comprehensive insights about PRN-1008 for immune thrombocytopenic purpura (ITP) in the seven major markets. A detailed picture of the PRN-1008 for ITP 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 PRN-1008 for ITP. 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 PRN-1008 market forecast analysis for ITP in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in ITP.
Rilzabrutinib (PRN-1008) is an orally administered reversible covalent inhibitor of bruton tyrosine kinase (BTK). BTK is an essential signaling element downstream of the B-cell receptor (BCR), Fc-gamma receptor, and Fc-epsilon receptor pathways. BTK activation is critical for B-cell activation and maturation. BTK also regulates antibody-mediated activation of other immune cells, such as macrophages, neutrophils, and mast cells, through Fc receptor signaling. The drug candidate is a fast-acting, orally available therapy that could effectively and safely modulate B-cell function without depleting the B-cell and is expected to be a major advancement in treating autoimmune and inflammatory diseases.
In preclinical studies, PRN1008 demonstrated a significant dose-dependent platelet loss reduction in an anti-CD41-induced mouse model of ITP. PRN1008 showed rapid and significant anti-inflammatory effects in an antibody-driven rat arthus model and spontaneous autoantibody-mediated canine pemphigus foliaceus. The preclinical data suggest that PRN1008 could reduce platelet destruction via inhibition of autoantibody/Fc-gamma receptor signaling in splenic macrophages and affect autoantibody generation effects on B-cell activation to diminish platelet loss in ITP.
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.
This report provides a detailed market assessment of PRN-1008 for immune thrombocytopenic purpura (ITP) 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 PRN-1008 for ITP covering trial interventions, trial conditions, trial status, start and completion dates.