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艾昆纬:2026年欧洲生物类似药可持续发展记分卡:总体概况及各国评分(英文版)(62页).pdf

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1、MAY2026Overall Summary and Country ScorecardsBiosimilar Sustainability Scorecards for Europe 2026IntroductionBiosimilar Sustainability Scorecards for Europe 2026:Overall Summary and Country ScorecardsAs biosimilars continue to play an expanding role in European healthcare systems,it is increasingly

2、important to understand not only the savings and access gains they generate,but also the market conditions required to maintain those benefits over time.IQVIA Institute published scorecards on the sustainability of biosimilar markets in 2018.This report aims to review this sustainability and how hea

3、lth care systems have evolved over time highlighting the positive levers and areas of development for biosimilar healthcare systems.This report highlights the value of biosimilars and evaluates the structural determinants of biosimilar market sustainability(i.e.long term viability of competition and

4、 supply)across a diverse set of European countries through a standardized,multi-dimensional assessment framework.It examines sixteen metrics across eight categories including pricing rules and dynamics,incentives,purchasing mechanisms,clinical guidelines and prescribing practices,competitive dynamic

5、s,and healthcare system performance to identify the policy configurations that support or hinder long-term biosimilar viability.By comparing country scorecards and underlying policy features,the analysis highlights where pricing compression,procurement rigidity,or weak incentive alignment may underm

6、ine manufacturer participation,as well as where balanced frameworks can sustain competition and access.The aim of the report is to inform stakeholders who are involved in the delivery and provision of to biosimilars such as policymakers,payers,healthcare professionals to industry stakeholders by ill

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1. **生物类似药价值**:截至2025年,欧洲生物类似药累计节省成本达750亿欧元(西欧640亿,中东欧110亿),治疗天数超90亿天,提升患者可及性(如英国扩大抗TNF疗法适用范围)。 2. **可持续性挑战**:2025-2032年将有24种原研生物药专利到期,但部分高价值分子(如帕博利珠单抗)缺乏生物类似药研发管线,存在市场风险。 3. **政策关键因素**:可持续性取决于定价规则(如强制降价、国际参考价)、采购机制(多中标方vs单一中标方)、激励措施(处方配额vs正向激励)等。平衡短期降价与长期市场活力(如德国、英国表现较好)至关重要。 4. **建议方向**:需优化采购模式(鼓励多中标方)、减少过度价格压力、完善临床指南,确保制造商参与度和供应安全。
生物类似药前景如何? 欧洲市场有何挑战? 如何保障可持续性?
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