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市場調査レポート
商品コード
1462291
エンテカビルの市場規模、予測、市場考察(2032年)Entecavir 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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エンテカビルの市場規模、予測、市場考察(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
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エンテカビルは強力かつ選択的なB型肝炎ウイルスの複製阻害剤です。HBe抗原陽性とHBe抗原陰性のラミブジン未治療のB型慢性肝炎(CHB)患者において、1日0.5mgのETV投与は、ラミブジン(LAM)と比較して、より強力なウイルス抑制、より高い生化学的寛解率、より良好な肝組織像の向上と関連しています。3年間のETV治療後、患者の大部分(94%)は、感度の高いPCRアッセイで検出されない血清HBV DNAレベルに達する可能性があります。LAM耐性HBV変異体を有する患者のETV治療では、1日1mgの高用量が必要ですが、3年後に強力なHBV抑制が達成されるのは40%に過ぎず、遺伝子型HBV耐性の累積率は1年目の6%から3年目には30%以上に増加します。ETVによるHBV耐性はラミブジン未治療患者ではまれであり、治療3年後の耐性率は1%未満と報告されています。結論として、ETVは耐性に対する遺伝的障壁が高い非常に強力な抗HBV薬であり、ラミブジン未治療のCHB患者において非常に有効であり、長期的な治療にはもっとも有望ですが、LAM耐性HBV変異体を保有するCHB患者にはあまり適していません。
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B型慢性肝炎向けエンテカビル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。
"Entecavir Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about entecavir for chronic hepatitis B in the seven major markets and China. A detailed picture of the entecavir 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 entecavir 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 entecavir 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.
Entecavir is a potent and selective inhibitor of hepatitis B virus replication. In HBeAg-positive and HBeAg-negative lamivudine-naive patients with chronic hepatitis B (CHB), treatment with ETV at a dose of 0.5 mg daily is associated with a more potent viral suppression, a higher rate of biochemical remission and a greater improvement of liver histology compared to Lamivudine (LAM). After 3 years of ETV treatment, the majority of patients (94%) may achieve serum HBV DNA levels undetectable by sensitive PCR assays. ETV treatment of patients with LAM-resistant HBV mutants requires a higher daily dose of 1 mg yet, potent HBV suppression at 3 years is achieved only in 40% of them while the cumulative rate of genotypic HBV resistance increases from 6% in the first year to >30% in year 3. ETV resistance of HBV is rare in lamivudine-naive patients with a reported rate of <1% after three years of treatment. In conclusion, ETV is a very potent anti-HBV drug with a high genetic barrier to resistance, highly effective in lamivudine-naive CHB patients and most promising for their long-term treatment but not very suitable for CHB patients harboring LAM-resistant HBV mutants.
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.
Entecavir Analytical Perspective by DelveInsight
This report provides a detailed market assessment of entecavir 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 entecavir for chronic hepatitis B covering trial interventions, trial conditions, trial status, start and completion dates.