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市場調査レポート
商品コード
1462317
VEMLIDY市場:市場規模、予測、市場洞察-2032年VEMLIDY Market Size, Forecast, and Market Insight - 2032 |
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カスタマイズ可能
適宜更新あり
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VEMLIDY市場:市場規模、予測、市場洞察-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
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VEMLIDYはHBVヌクレオシド類似体逆転写酵素阻害剤であり、成人および12歳以上の代償性肝疾患を有する小児患者における慢性B型肝炎ウイルス感染の治療に適応があります。
VEMLIDYは新規のテノホビルの標的プロドラッグで、GileadのVIREAD(テノホビルジソプロキシルフマル酸塩、TDF)300mgと同様の抗ウイルス効果を示し、その用量はGileadのVIREAD(テノホビルジソプロキシルフマル酸塩、TDF)300mgの10分の1以下です。製品ラベルには、乳酸アシドーシス/脂肪症を伴う重篤な肝腫大、および治療後のB型肝炎の重篤な急性増悪のリスクに関する枠付き警告が記載されています。
今後数年間で、慢性B型肝炎の市場シナリオは、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、VEMLIDY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。慢性B型肝炎を対象とした他の新興製品がVEMLIDYと厳しい市場競争を繰り広げることが予想され、近い将来、後発の新興治療薬が上市されれば、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ヶ国および中国における慢性B型肝炎治療薬のVEMLIDY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。
"VEMLIDY Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about VEMLIDY for chronic hepatitis B in the seven major markets and China. A detailed picture of the VEMLIDY for chronic hepatitis B in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, Japan, and China for the study period 2019 -2032 is provided in this report along with a detailed description of the VEMLIDY for chronic hepatitis B. 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 VEMLIDY market forecast analysis for chronic hepatitis B in the 7MM and China, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in chronic hepatitis B.
VEMLIDY is a HBV nucleoside analog reverse transcriptase inhibitor and is indicated for treating chronic hepatitis B virus infection in adults and pediatric patients 12 years and older with compensated liver disease.
VEMLIDY is a novel, targeted prodrug of tenofovir that has demonstrated antiviral efficacy similar to and at a dose less than one-tenth that of Gilead's VIREAD (tenofovir disoproxil fumarate, TDF) 300 mg. It has a boxed warning on its product label regarding the risks of lactic acidosis/severe hepatomegaly with steatosis and post-treatment severe acute exacerbation of hepatitis B.
The recommended dosage of VEMLIDY in adults and pediatric patients aged 12 and older is one 25 mg tablet taken orally once daily with food.
Tenofovir alafenamide is an antiviral drug against the hepatitis B virus; it is a phosphonamidate prodrug of tenofovir (2'-deoxyadenosine monophosphate analog). Tenofovir alafenamide is a lipophilic cell-permeate compound that enters primary hepatocytes by passive diffusion and hepatic uptake transporters OATP1B1 and OATP1B3. It is then converted to tenofovir through hydrolysis, primarily by carboxylesterase 1 (CES1) in primary hepatocytes. Intracellular tenofovir is subsequently phosphorylated by cellular kinases to the pharmacologically active metabolite tenofovir diphosphate. Tenofovir diphosphate inhibits HBV replication through incorporation into viral DNA by the HBV reverse transcriptase, which results in DNA chain termination.
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.
VEMLIDY Analytical Perspective by DelveInsight
This report provides a detailed market assessment of VEMLIDY for chronic hepatitis B in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, Japan, and China. This segment of the report provides forecasted sales data from 2024 to 2032.
The report provides the clinical trials information of VEMLIDY for chronic hepatitis B covering trial interventions, trial conditions, trial status, start and completion dates.