![]() |
市場調査レポート
商品コード
1462320
WAYLIVRAの市場規模、予測、新薬の考察(2032年)WAYLIVRA Market Size, Forecast, and Emerging Insight - 2032 |
||||||
カスタマイズ可能
適宜更新あり
|
WAYLIVRAの市場規模、予測、新薬の考察(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
|
アポリポタンパクCIII(apoCIII)mRNAのアンチセンスオリゴヌクレオチド阻害薬であるWAYLIVRA(ボラネソーセン)は、家族性部分性脂肪萎縮症(FPL)の治療薬として、Ionis Pharmaceuticalsが子会社のAkcea Therapeuticsを通じて開発中です。家族性部分性脂肪萎縮症(FPL)は、身体のさまざまな部位から選択的かつ進行性に体脂肪(脂肪組織)が減少することを特徴とする稀な遺伝性疾患です。FPL患者は、腕や脚の皮下脂肪が減少していることが多く、頭部や体幹部で脂肪が減少している場合とそうでない場合があります。この薬剤は脂肪萎縮症治療薬としてブラジルでの上市承認を取得しており、米国、欧州、日本で臨床開発中です。
ボラネソーセンはアンチセンスオリゴヌクレオチドで、アポC-III mRNAに結合し、その分解を誘導し、アポC-IIIタンパク質の翻訳を阻害します。通常、アポC-IIIはトリグリセリド代謝とカイロミクロンの肝クリアランスを阻害します。アポC-IIIの翻訳を阻止することにより、これらのトリグリセリドとカイロミクロンの代謝と分解が可能になります。
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)における脂肪萎縮症向けWAYLIVRA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。
"WAYLIVRA Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about WAYLIVRA for lipodystrophy in the seven major markets. A detailed picture of the WAYLIVRA for lipodystrophy 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 WAYLIVRA for lipodystrophy. 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 WAYLIVRA market forecast analysis for lipodystrophy in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in lipodystrophy.
WAYLIVRA (volanesorsen), an antisense oligonucleotide inhibitor of apolipoprotein CIII (apoCIII) mRNA, is being developed by Ionis Pharmaceuticals through its subsidiary company, Akcea Therapeutics to treat familial partial lipodystrophy (FPL). Familial partial lipodystrophy (FPL) is a rare genetic disorder characterized by selective, progressive body fat loss (adipose tissue) from various body areas. Individuals with FPL often have reduced subcutaneous fat in the arms and legs, and the head and trunk regions may or may not have fat loss. The drug received marketing approval in Brazil for the treatment of lipodystrophy and is investigated under clinical development in the US, Europe and Japan.
Volanesorsen is an antisense oligonucleotide that binds to apoC-III mRNA, leading to its degradation and preventing the translation of apoC-III protein. Normally, apoC-III would inhibit triglyceride metabolism and hepatic clearance of chylomicrons. Preventing translation of apoC-III allows for the metabolism and breakdown of these triglycerides and chylomicrons.
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.
WAYLIVRA Analytical Perspective by DelveInsight
This report provides a detailed market assessment of WAYLIVRA for lipodystrophy 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 WAYLIVRA for lipodystrophy covering trial interventions, trial conditions, trial status, start and completion dates.