市場調査レポート
商品コード
1462267
P2B-001の市場規模、予測、新薬の考察(2032年)P2B-001 Market Size, Forecast, and Emerging Insight - 2032 |
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P2B-001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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Pharma Two Bが開発中のP2B-001は、低用量ドパミン作動薬である徐放性プラミペキソールと低用量モノアミン酸化酵素B(MAO-B)阻害薬であるラサギリンの新しい1日1回投与の併用療法であり、パーキンソン病治療薬として特別に開発されました。
この2つの薬剤は、互いに助け合う2つの異なるメカニズムで作用するため、併用することでそれぞれの薬剤よりも優れた効果が得られると考えられる理由があります。治療効果を失うことなく、より低用量で使用することができます。したがって、P2B001の開発は、改良された製剤でこれら2つの薬剤の低用量の組み合わせを提供することを意図しており、それぞれの薬剤を単独で服用したり、現在市販されている薬剤を併用したりするよりも、パーキンソン病の症状を抑制する効果が高く、副作用が少ないと期待されています。
Pharma Two Bは、P2B001の早期パーキンソン病に対する1日1回、無滴定の治療薬としての有効性と安全性を調査するフェーズIIb試験とフェーズIII試験を完了しました。FDAへのNDA申請が準備中です。すでに終了した臨床試験では、P2B001を投与された患者において、プラセボを投与された患者と比較してパーキンソン病症状の有意な改善が認められました。
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)におけるパーキンソン病向けP2B-001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。
"P2B-001 Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about P2B-001 for Parkinson's disease in the seven major markets. A detailed picture of the P2B-001 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 P2B-001 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 P2B-001 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.
P2B-001 being developed by Pharma Two B, is a novel, once-daily combination of extended-release pramipexole, a low-dose dopamine agonist, and rasagiline, a low-dose Monoamine Oxidase-B (MAO-B) inhibitor, developed specifically for the treatment of Parkinson's disease.
The two drugs work in two different mechanisms that help each other, so there is a reason to believe that their combined activity will be better than each drug. Lower doses can be used without losing the therapeutic effect. Thus, the development of P2B001 is intended to provide a combination of low doses of these two drugs in an improved formulation that is hoped to be more effective in controlling Parkinson's disease symptoms and with fewer side effects than each of the drugs taken alone or the currently available commercial drugs taken together.
Pharma Two B has completed Phase IIb and Phase III studies investigating P2B001's efficacy and safety as a once-daily, no-titration treatment for early-stage Parkinson's disease. An NDA submission to the FDA is being prepared. In a previously completed clinical trial, a significant improvement in Parkinson's disease symptoms was seen in patients treated with P2B001 compared to patients that were treated with a placebo.
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.
P2B-001 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of P2B-001 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 P2B-001 for Parkinson's disease covering trial interventions, trial conditions, trial status, start and completion dates.