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美国具有多个生物类似药竞争者的生物市场动态。

Dynamics of biological markets with multiple biosimilar competitors in the United States.

机构信息

The Hilltop Institute, University of Maryland, Baltimore County, MD, USA.

Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

出版信息

Expert Opin Biol Ther. 2024 Nov;24(11):1271-1278. doi: 10.1080/14712598.2024.2412648. Epub 2024 Oct 9.

Abstract

BACKGROUND

The dynamics of biological markets with multiple biosimilar competitors in the United States are poorly understood. Moreover, due to confidentiality issues, the relationship between originator biologic net prices, rebates, and biosimilar entry is largely unexplored.

RESEARCH DESIGN AND METHODS

We conducted a review of the Food Drug Administration (FDA) purple book and manufacturer websites to identify all originator biologics with multiple competitors and their characteristics. We leveraged a novel data source to examine originator biologic net prices and rebates over time and used descriptive statistics and interrupted time-series analyses to assess their relationship with biosimilar entry.

RESULTS

By December 2022, only five originator biologics had three or more available biosimilar competitors. Mean time between biosimilar approval and biosimilar launch was 9 months (SD = 7.04 months). By third biosimilar competitor, entry net prices for originator biologics had decreased by 9.34% to 50.93%, while rebates had increased by 25.35% to 89.71%.

CONCLUSIONS

Very few originator biologics have multiple available biosimilar competitors. Barrier to biosimilar availability seems to be at the approval level as the time between approval and launch is relatively short. However, originator biologics respond quickly to biosimilar competition, mainly through an increase in rebates.

摘要

背景

美国多个生物类似药竞争产品的生物市场动态尚未得到充分了解。此外,由于保密性问题,原研生物制剂净价、回扣与生物类似药进入市场之间的关系在很大程度上仍未得到探索。

研究设计与方法

我们对食品和药物管理局(FDA)的紫皮书和制造商网站进行了审查,以确定所有具有多个竞争产品的原研生物制剂及其特征。我们利用一个新颖的数据来源来研究原研生物制剂的净价和回扣随时间的变化情况,并使用描述性统计和中断时间序列分析来评估它们与生物类似药进入市场之间的关系。

结果

截至 2022 年 12 月,只有 5 种原研生物制剂有 3 种或更多种可获得的生物类似药竞争产品。生物类似药获得批准与开始销售之间的平均时间为 9 个月(SD=7.04 个月)。到第三个生物类似药竞争产品时,原研生物制剂的进入净价已下降 9.34%至 50.93%,而回扣则增加了 25.35%至 89.71%。

结论

很少有原研生物制剂有多个可获得的生物类似药竞争产品。生物类似药的可用性似乎存在障碍,因为批准和上市之间的时间相对较短。然而,原研生物制剂对生物类似药竞争的反应很快,主要是通过增加回扣来实现。

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