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市場調査レポート
商品コード
1381084
FLUCELVAX QUADRIVALENTの薬剤に関する洞察と市場予測:2032年FLUCELVAX QUADRIVALENT Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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FLUCELVAX QUADRIVALENTの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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FLUCELVAX QUADRIVALENT(インフルエンザワクチン)は、連続細胞株であるMDCK(Madin Darby Canine Kidney)細胞で増殖させた細胞由来候補ワクチンウイルス(CVV)を用いて製造されたサブユニットインフルエンザワクチンです。これらの細胞は、培養液中で懸濁状態で自由に増殖するように適合されています。ウイルスはB-プロピオラクトンで不活化され、洗浄剤の臭化セチルトリメチルアンモニウムで破壊され、いくつかの工程を経て精製されます。4種類のウイルス株はそれぞれ製造され、別々に精製された後、4価ワクチンを製造するためにプールされます。
2019年、同社は欧州委員会が新しい細胞ベースの季節性インフルエンザワクチンであるFLUCELVAX TETRAインフルエンザの販売承認を発行したと発表しました。
今後数年間で、季節性インフルエンザの市場シナリオは、世界中の広範な研究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、FLUCELVAX QUADRIVALENT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。季節性インフルエンザに対する他の新興製品は、FLUCELVAX QUADRIVALENTに厳しい市場競合を与えることが予想され、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6ヶ国におけるFLUCELVAX QUADRIVALENT市場について調査し、市場の概要とともに、2023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。
“"FLUCELVAX QUADRIVALENT Drug Insight and Market Forecast - 2032" report provides comprehensive insights about FLUCELVAX QUADRIVALENT for seasonal influenza in the six major markets. A detailed picture of the FLUCELVAX QUADRIVALENT for seasonal influenza in the 6MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom for the study period 2019 -2032 is provided in this report along with a detailed description of the FLUCELVAX QUADRIVALENT for seasonal influenza. 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 FLUCELVAX QUADRIVALENT market forecast analysis for seasonal influenza in the 6MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in seasonal influenza.
FLUCELVAX QUADRIVALENT (influenza vaccine) is a subunit influenza vaccine manufactured using cell-derived candidate vaccine viruses (CVV) that are propagated in Madin Darby Canine Kidney (MDCK) cells, a continuous cell line. These cells were adapted to grow freely in suspension in a culture medium. The virus is inactivated with B-propiolactone, disrupted by the detergent cetyltrimethylammonium bromide, and purified through several process steps. Each of the four virus strains is produced, purified separately, and then pooled to formulate the quadrivalent vaccine.
In 2019, the company announced that European Commission has issued marketing approval for its new cell-based seasonal influenza vaccine, FLUCELVAX TETRA influenza, the first cell-based quadrivalent influenza vaccine (QIVc) available in Europe and is licensed for use in people 9 years and above.
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 FLUCELVAX QUADRIVALENT for seasonal influenza in the six major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom. This segment of the report provides forecasted sales data from 2023 to 2032.
The report provides the clinical trials information of FLUCELVAX QUADRIVALENT for seasonal influenza covering trial interventions, trial conditions, trial status, start and completion dates.