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시장보고서
상품코드
2064037
ENTYVIO : 판매 예측 및 시장 규모(2034년)ENTYVIO Sales Forecast, and Market Size Analysis - 2034 |
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DelveInsight
ENTYVIO는 여전히 다케다의 주요 성장 브랜드 중 하나입니다. 다케다(Takeda)는 2023/24 회계연도 ENTYVIO의 전 세계 매출이 약 7,460억 엔(약 50억 달러)이었다고 보고했으며, 여러 지역에서 지속적인 두 자릿수 실질 성장을 기록하고 있습니다. 2024년도 분기 보고서에서는 주요 시장에서 전년 동기 대비 약 13-17%의 성장률이 나타났습니다.
다케다는 기존 제품의 독점 판매권이 상실되는 상황에서 ENTYVIO를 장기적인 성장의 주요 원동력으로 삼고 있습니다.
이러한 성장의 주요 요인은 궤양성 대장염 및 크론병의 유지 요법을 대상으로 한 피하 주사제 ENTYVIO 펜에 대한 FDA 승인입니다. 피하 주사제를 통해 환자는 2주마다 집에서 스스로 투여할 수 있게 되어, 정맥 주사 시설에 대한 의존도를 줄이고 편의성을 높일 수 있습니다.
크론병을 대상으로 한 주요 VISIBLE 2 임상시험에서는:
피하 투여로 전환함에 따라 환자의 치료 지속률이 향상되고, 전 세계에서 의료진의 채택이 확대될 것으로 기대됩니다.
ENTYVIO는 다음과 같은 적응증으로 승인되었습니다. :
전 세계 IBD(염증성장질환)의 유병률은 계속 증가하고 있으며, 특히 북미, 유럽, 아시아·태평양 지역에서 이러한 경향이 두드러지고 있습니다. 진단율의 상승과 생물제제의 조기 사용 확대가 베돌리주맙과 같은 첨단 치료제에 대한 지속적인 수요를 지원하고 있습니다.
ENTYVIO는 소화관 내의 α4B7 인테그린 경로를 특이적으로 표적으로 삼아, 전신적인 면역 억제를 최소화하면서 장의 염증을 완화합니다.
이러한 장 선택적 작용 기전은 전신성 면역억제 작용을 가진 생물제제나 JAK 억제제 사용에 따른 감염 위험을 우려하는 환자와 의사들에게 특히 큰 경쟁 우위를 제공합니다. 우수한 장기 안전성 프로파일 덕분에 조기 치료 및 유지 요법으로서의 사용이 확대되고 있습니다.
장기적인 관해 유지 효과와 내약성이 임상 현장에서의 도입을 지속적으로 지원하고 있습니다. 실제 임상 현장에서 의사의 경험과 환자 보고 결과(PRO)는 특히 생물제제 사용 경험이 있는 환자들 사이에서 ENTYVIO에 대한 신뢰를 더욱 공고히 하고 있습니다.
ENTYVIO의 최근 동향
이 보고서는 주요 7개국(미국, EU 4개국(독일, 프랑스, 이탈리아, 스페인), 영국, 일본)에서 ENTYVIO의 동향을 조사하여, 크론병, 포치염, 궤양성 대장염과 같은 승인된 적응증은 물론, 이식편 대 숙주 질환 및 셀리악병 등의 잠재적 적응증에 관한 포괄적인 인사이트를 제공합니다.
이 보고서에서는 2020-2034년 승인된 적응증에 대한 기존 사용 현황, 잠재적 적응증으로의 진출 전망, 시장 성과에 대한 상세한 분석과 더불어, 승인된 적응증 및 잠재적 적응증에 대한 ENTYVIO의 상세한 설명이 제공됩니다. 또한 ENTYVIO의 매출 전망, 작용 기전(MoA), 투여량 및 투여 방법, 규제 관련 주요 단계 등을 포함한 연구개발 및 기타 활동에 대한 인사이트, 향후 시장 평가, SWOT 분석, 애널리스트의 견해, 경쟁 구도, 각 적응증별 기타 신흥 치료제에 대한 개요, 시장을 촉진하는 요인에 대해서도 분석하고 있습니다.
ENTYVIO remains one of Takeda's top growth brands. Takeda reported FY2023/24 ENTYVIO sales of approximately ¥746 billion (~US$5 billion) globally, reflecting continued double-digit operational growth in several regions. Quarterly reports during FY2024 highlighted growth rates of approximately 13-17% year-over-year in major markets.
Takeda continues to position ENTYVIO as a key long-term growth driver as legacy products lose exclusivity.
A major catalyst has been the FDA approval of subcutaneous ENTYVIO Pen for both UC and Crohn's disease maintenance therapy. The SC formulation allows patients to self-administer treatment at home every two weeks, reducing infusion-center dependence and improving convenience.
In the pivotal VISIBLE 2 trial for Crohn's disease:
The SC transition is expected to improve patient retention and broaden physician adoption globally.
ENTYVIO is approved for:
Global IBD prevalence continues to rise, particularly in North America, Europe, and increasingly in Asia-Pacific regions. Growing diagnosis rates and earlier biologic use are supporting sustained demand for advanced therapies such as vedolizumab.
ENTYVIO specifically targets the a4B7 integrin pathway in the gastrointestinal tract, reducing gut inflammation while limiting systemic immunosuppression.
This gut-selective mechanism has become a major competitive advantage, especially for patients and physicians concerned about infection risks associated with systemic immunosuppressive biologics and JAK inhibitors. The favorable long-term safety profile has strengthened its use as both earlier-line and maintenance therapy.
Long-term remission durability and tolerability continue to drive adoption in clinical practice. Real-world physician experience and patient-reported outcomes have reinforced confidence in ENTYVIO, especially among biologic-experienced patients.
ENTYVIO Recent Developments
"ENTYVIO Sales Forecast, and Market Size Analysis - 2034" report provides comprehensive insights of ENTYVIO for approved indication like Crohn's disease, Pouchitis and Ulcerative colitis; as well as potential indication like Graft-versus-host disease and Coeliac disease in the 7MM. A detailed picture of ENTYVIO's existing usage in approved and anticipated entry and performance in potential indications in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2020 -2034 is provided in this report along with a detailed description of the ENTYVIO for approved and potential indications. The ENTYVIO market report provides insights about ENTYVIO's sales forecast, mechanism of action (MoA), dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of historical and current ENTYVIO performance, future market assessments inclusive of the ENTYVIO market forecast analysis for approved and potential indications in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in respective indications. It also provides analysis of ENTYVIO sales forecasts, along with factors driving its market.
ENTYVIO Drug Summary
ENTYVIO is a gut-selective biologic therapy developed by Takeda Pharmaceutical Company for the treatment of moderately to severely active ulcerative colitis and Crohn's disease in adults. It is a humanized monoclonal antibody that specifically targets the a4B7 integrin on lymphocytes, blocking their interaction with MAdCAM-1 and thereby preventing inflammatory immune cells from migrating into gastrointestinal tissue, which helps reduce chronic gut inflammation while minimizing systemic immunosuppression. ENTYVIO is available as both intravenous infusion and subcutaneous injection formulations, offering flexible maintenance therapy options for patients with inflammatory bowel disease (IBD). Approved initially in 2014, the drug has demonstrated strong efficacy in inducing and maintaining clinical remission through pivotal GEMINI studies and is recognized for its favorable safety profile compared with broader immunosuppressive biologics, particularly due to its gut-selective mechanism. Common adverse events include headache, nasopharyngitis, arthralgia, nausea, and upper respiratory infections, while patients are also monitored for infection risk and hypersensitivity reactions during therapy. The report provides ENTYVIO's sales, growth barriers and drivers, post usage and approvals in multiple indications.
Scope of the ENTYVIO Market Report
The report provides insights into:
The ENTYVIO market 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.
ENTYVIO Analytical Perspective by DelveInsight
This ENTYVIO sales market forecast report provides a detailed market assessment of ENTYVIO for approved indication like Crohn's disease, Pouchitis and Ulcerative colitis; as well as potential indication like Graft-versus-host disease and Coeliac disease 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 current and forecasted ENTYVIO sales data uptil 2034.
The ENTYVIO market report provides the clinical trials information of ENTYVIO for approved and potential indications covering trial interventions, trial conditions, trial status, start and completion dates.
ENTYVIO Competitive Landscape
The report provides Insights on competitors and marketed products within the domain, along with a summary of emerging products and their respective launch dates, posing significant competition in the market.
ENTYVIO Market Potential & Revenue Forecast
ENTYVIO Competitive Intelligence
ENTYVIO Regulatory & Commercial Milestones
ENTYVIO Clinical Differentiation
ENTYVIO Market Report Highlights