市場調査レポート
商品コード
1462269
Buntanetap市場:市場規模、予測、新たな洞察- 2032年Buntanetap Market Size, Forecast, and Emerging Insight - 2032 |
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Buntanetap市場:市場規模、予測、新たな洞察- 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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Buntanetap(旧名:ANVS401またはポジフェン)は、合成経口神経毒性凝集タンパク質(TINAPs)阻害剤であり、神経毒性タンパク質のレベルを低下させ、結果として脳内の毒性を軽減します。Buntanetapは経口投与可能な低分子化合物で、そのユニークな作用機序により、神経変性の主原因の一つである複数の神経毒性タンパク質-APP/AB(APP)、タウ/ホスホ-タウ(タウ)、a-シヌクレイン(aSYN)-を一度に阻害し、運動機能を改善することができます。
米国FDAは、早期および進行パーキンソン病に対するBuntanetapの第III相試験への開発継続を承認しました。現在、Buntanetapは早期パーキンソン病の第III相試験で研究されており、同社は2023年末までに試験を完了する予定です。同社はまた、アルツハイマー病やその他の神経変性疾患に対してもBuntanetapを開発しています。
今後数年間で、パーキンソン病の市場シナリオは、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、病状を治療/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、Buntanetap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。パーキンソン病に対する他の新興製品は、Buntanetapとの厳しい市場競争になると予想され、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ヶ国におけるパーキンソン病治療薬のBuntanetap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。
"Buntanetap Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about buntanetap for Parkinson's disease in the seven major markets. A detailed picture of the buntanetap for Parkinson's Disease 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 buntanetap for Parkinson's Disease. 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 buntanetap market forecast analysis for Parkinson's disease in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Parkinson's disease.
Buntanetap (previously known as ANVS401 or posiphen) is a synthetically produced oral translational inhibitor of neurotoxic aggregating proteins (TINAPs), which lowers the level of neurotoxic proteins and consequently less toxicity in the brain. Buntanetap is an orally available small molecule, and its unique mechanism of action allows it to inhibit multiple neurotoxic proteins-APP/AB (APP), tau/phospho-tau (tau), and a-Synuclein (aSYN)-that is one of the main causes of neurodegeneration at once and improve motor function.
The US FDA has green-lighted the continued development of Buntanetap into phase III for early and advanced Parkinson's disease. Presently buntanetap is being studied in a Phase III early Parkinson's disease study and the company expects to complete the trial by the end of 2023. The company is also developing buntanetap for Alzheimer's disease and other neurodegenerative 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.
Buntanetap Analytical Perspective by DelveInsight
This report provides a detailed market assessment of buntanetap for Parkinson's disease 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 buntanetap for Parkinson's disease covering trial interventions, trial conditions, trial status, start and completion dates.