关于FDA批准的胰岛素产品的专利和监管独家权:一项纵向数据库研究,1986-2019年
Anders Olsen1,2, Reed F Beall1,3, Ryan P Knox1,4
1Program On Regulation, Therapeutics, And Law, Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS medicine
|November 16, 2023
概括
胰岛素制造商通过在FDA批准后申请专利来扩大市场独家权,特别是在输送设备上. 政策改革是必要的,以确保患者获得负担得起的胰岛素药物.
科学领域:
- 制药科学 制药科学
- 卫生政策 卫生政策
- 药物开发 药物开发
背景情况:
- 胰岛素仍然是糖尿病的关键治疗方法,但在美国面临着高昂的成本.
- 胰岛素的市场排他性通常通过专利和监管排他性来延长.
- 这限制了竞争,并导致药品价格上.
研究的目的:
- 调查制造商如何利用专利和监管独家权.
- 审查1986年至2019年间批准的胰岛素产品市场独家权的扩展.
- 了解对竞争和药品定价的影响.
主要方法:
- 利用FDA的色书来识别批准的生物合成胰岛素产品.
- 对每个产品的记录专利和监管独家权.
- 使用谷歌专利分析了专利时间和重点 (例如,交付设备).
- 计算了预期市场保护的持续时间.
主要成果:
- 胰岛素产品预期保护的中位持续时间为16.0年.
- 在FDA批准后提交的专利将某些产品的保护期限平均延长了6年.
- 大约63%的药物设备组合专利与输送设备有关.
结论:
- 胰岛素制造商采用诸如批准后专利和输送设备的广泛专利等策略,以扩大市场排他性.
- 这些做法导致了基本糖尿病药物持续高昂的成本.
- 建议进行政策改革,以促进竞争并改善患者获得负担得起的胰岛素.
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