捕捉欧洲生物类似药的整体价值 - - 第一部分:历史视角
Jorge Mestre-Ferrandiz1, Marcin Czech2, Josef S Smolen3
1Department of Economics, Universidad Carlos III, Madrid, Spain.
Expert review of pharmacoeconomics & outcomes research
|January 4, 2024
概括
生物仿制药提高了患者在欧洲获得创新的生物治疗的机会. 这增加了更多患者的治疗选择和持续时间,改善了整体结果.
科学领域:
- 药物经济学和卫生政策
- 生物制药市场分析分析
- 临床获得治疗药物的机会.
背景情况:
- 已批准的生物仿制药的疗效,安全性和免疫性与参考生物药物具有相似的效果.
- 了解欧洲生物仿制药的社会价值和市场动态对于优化治疗机会至关重要.
研究的目的:
- 收集欧洲利益相关者关于生物类似药物的影响的观点.
- 确定影响生物类似药市场动态和采用因素.
- 评估生物类似药在欧洲医疗保健系统中的社会价值.
主要方法:
- 与欧洲临床医生,药剂师和付款人 (N=103) 进行了一项独立调查和深入采访.
- 一个专家小组为生物类似药的采用制定了市场成熟度框架.
- 研究结果与现有出版文献进行了背景化.
主要成果:
- 受访者认为生物仿制药是增加获得创新药物 (73%) 和生物治疗 (66%) 的关键驱动因素.
- 生物相似竞争与生物制剂 (50%) 的扩大获取,药物组合 (36%) 和减少获取时间 (34%) 相关.
- 增加生物意识 (51%) 和更新的处方指南 (37%) 被确定为生物类似物进入后生物接触的主要促进因素.
结论:
- 欧洲的利益相关者认为,生物类似药可以通过提高获得生物药物和创新疗法的机会,显著改善患者的治疗结果.
- 生物类似药物有助于为更广泛的患者群体提供更早,更持续的治疗.
- 该研究强调了生物类似药在扩大医疗保健选择方面对社会产生积极影响.
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