|
시장보고서
상품코드
1462291
엔테카비르 시장 규모, 예측, 시장 인사이트(2032년)Entecavir Market Size, Forecast, and Market Insight - 2032 |
||||||
엔테카비르는 강력하고 선택적인 B형 간염 바이러스 복제 억제제이며, HBe 항원 양성 및 HBe 항원 음성인 라미부딘 미치료 만성 B형 간염(CHB) 환자에서 매일 0.5mg의 ETV 투여는 라미부딘(LAM)과 비교하여 더 강력한 바이러스 억제, 더 높은 생화학적 완화율, 개선된 간 조직 영상과 관련이 있습니다. 3년간의 ETV 치료 후 대부분의 환자(94%)는 민감한 PCR 분석에서 검출되지 않는 혈청 HBV DNA 수준에 도달 할 수 있으며, LAM 내성 HBV 변이체를 가진 환자의 ETV 치료에는 하루 1mg의 고용량이 필요합니다. 그러나 3년후 강력한 HBV 억제율은 40%에 불과하고 유전자형 HBV 내성의 누적 비율은 1년차 6%에서 3년차에는 30% 이상으로 증가하며 ETV에 의한 HBV 내성은 라미부딘 미치료 환자에서 드물며 치료 3년후 내성률은 1% 미만인 것으로보고되었습니다. 결론적으로, ETV는 내성에 대한 유전적 장벽이 높은 매우 강력한 항HBV 약물로, 라미부딘 미치료 CHB 환자에서 매우 효과적이며 장기적인 치료에 가장 유망하지만, LAM 내성 HBV 변이체를 보유한 CHB 환자에게는 적합하지 않습니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 B형 만성 간염용 엔테카비르에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"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.