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시장보고서
상품코드
1614794
Vonafexor 시장 : 시장 규모, 예측, 새로운 인사이트(-2032년)Vonafexor Market Size, Forecast, and Emerging Insight - 2032 |
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Vonafexor(EYP001)는 경구 투여 가능한 비 스테로이드성 합성 담즙산 FXR 작용제로 NASH 치료제로 개발 된 저분자 화합물입니다. FXR 작용제가 미래의 NASH 치료의 핵심 약물이 될 수 있다는 것은 많은 KOL이 인정합니다. 스테릭 마우스 모델 STAM에서 대부분의 NASH 주요 매개 변수(섬유화, 지방증, 염증, 풍선 형성, 트리글리세라이드, NAS)에 유의 한 긍정적인 영향을 미치고 그 효과를 입증합니다. 이 약은 다른 FXR 작용제와는 다른 독특한 화학적 특성과 PK PD 프로파일을 가지며 동급 최고의 치료 지표를 제공할 수 있습니다.
Vonafexor(EYP001)는 현재 진행성 NASH, 즉 섬유화 단계 F2 또는 F3 환자를 대상으로 하는 2a상 임상시험에서 평가되고 있습니다. 중간안전성 분석의 결과, 양호한 내약성이 확인되었기 때문에 독립위원회(DSMC)는 예정대로 임상시험을 완료할 것을 제안했습니다. 만성 B형 간염과 NASH를 대상으로, 주요 화합물 Vonafexor의 3가지 2상 임상시험이 실시되었습니다.
본 보고서는 주요 7개국에서의 Vonafexor 시장을 조사했으며, 시장 개요와 함께 경쟁 구도, 2032년까지 시장 규모 예측, 국가별 시장 분석 등을 제공합니다.
"Vonafexor Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about Vonafexor for Non-alcoholic Steatohepatitis (NASH) in the seven major markets. A detailed picture of the Vonafexor for NASH 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 Vonafexor for NASH. 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 Vonafexor market forecast analysis for NASH in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in NASH.
Vonafexor (EYP001) is an orally bioavailable synthetic non-steroidal, non-bile acid FXR agonist small molecule also developed in NASH. Most KOL agrees that FXR agonists could become the backbone of future NASH therapies. It has demonstrated its efficacy in a stelic mouse model STAM with a significant positive impact on most NASH key parameters (fibrosis, steatosis, inflammation, ballooning, triglycerides, and NAS). It differentiates from other FXR agonists with a unique chemistry and PK PD profile to possibly provide a best-in-class therapeutic index.
Vonafexor (EYP001) is currently evaluated in a Phase IIa clinical trial in patients with advanced NASH, i.e., a fibrosis Stage F2 or F3. After the interim safety analysis showed good tolerance, the independent DSMC suggested pursuing the trial to completion as planned. The company conducts three Phase II trials with its lead compound Vonafexor in Chronic Hepatitis B and NASH.
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.
Vonafexor Analytical Perspective by DelveInsight
This report provides a detailed market assessment of Vonafexor for Non-alcoholic Steatohepatitis (NASH) 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 2027 to 2032.
The report provides the clinical trials information of Vonafexor for Non-alcoholic Steatohepatitis (NASH) covering trial interventions, trial conditions, trial status, start and completion dates.