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1995 年至 2014 年美国食品和药物管理局批准的新型治疗药物的销售额。

Sales Revenues for New Therapeutic Agents Approved by the United States Food and Drug Administration From 1995 to 2014.

机构信息

Department of Health Policy, London School of Economics and Political Science, London, England, UK.

Program on Regulation, Therapeutics, and Law, Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Value Health. 2024 Oct;27(10):1373-1381. doi: 10.1016/j.jval.2024.06.015. Epub 2024 Jul 6.

Abstract

OBJECTIVES

This study aimed to analyze worldwide sales of new therapeutic agents and to estimate the time it takes for product sales to exceed industry-wide average drug development costs.

METHODS

Data obtained from company reports were analyzed to track worldwide sales of new medicines approved by the US Food and Drug Administration from 1995 to 2014. All sales figures were reported in 2019 US dollars. Kaplan-Meier curves were used to evaluate the time it took for discounted product sales to exceed the average costs associated with developing 1 new drug (accounting for the costs of failed trials), using published estimates of these costs.

RESULTS

Based on data for 361 of 558 new therapeutic agents approved over the study period (median follow-up 13.2 years), mean sales revenue per product was $15.2 billion through the end of 2019; the median was $6.7 billion. These products jointly generated global sales of $5.5 trillion since approval. Revenues were highly skewed, with the 25 best selling products (7%, 25 of 361) accounting for 38% of this amount ($2.1 trillion of $5.5 trillion). Approximately 47% of products had discounted sales that exceeded the estimated industry-wide average costs of development within 5 years of approval, and 75% within 10 years. After attributing potential production, marketing, and other costs, these numbers dropped to 21% of products within 5 years of approval, and 46% within 10 years.

CONCLUSIONS

Sales of new medicines approved from 1995 to 2014 were highly skewed, but many products had net discounted sales that exceeded the industry-wide average costs of development within 10 years of approval. An understanding of how sales revenues accrue in the years after initial approval, alongside data on business costs, can inform discussions about how to incentivize private investment in innovation while ensuring affordable prices for patients and the healthcare system.

摘要

目的

本研究旨在分析全球新治疗药物的销售情况,并估算产品销售额超过行业内平均药物研发成本所需的时间。

方法

从公司报告中获取数据,以跟踪 1995 年至 2014 年期间经美国食品和药物管理局批准的新药的全球销售情况。所有销售数据均以 2019 年的美元报告。使用已发表的这些成本估算值,通过 Kaplan-Meier 曲线评估折扣后产品销售额超过开发 1 种新药(考虑到失败试验的成本)相关平均成本所需的时间,其中 1 种新药的成本。

结果

根据研究期间批准的 558 种新治疗药物中的 361 种药物的数据(中位随访时间为 13.2 年),截至 2019 年底,每个产品的平均销售收益为 152 亿美元;中位数为 67 亿美元。这些产品自批准以来共产生了 5500 亿美元的全球销售额。收入高度偏态分布,25 种畅销产品(7%,361 种中的 25 种)占销售额的 38%(5500 亿美元中的 2100 亿美元)。大约 47%的产品在批准后 5 年内的折扣销售额超过了估计的行业平均研发成本,75%的产品在 10 年内超过了这一成本。在考虑潜在的生产、营销和其他成本后,这些数字在批准后 5 年内降至 21%的产品,在 10 年内降至 46%的产品。

结论

1995 年至 2014 年批准的新药销售情况高度偏态分布,但许多产品在批准后 10 年内的折扣销售额超过了行业平均研发成本。了解初始批准后几年内销售收入的积累情况,以及有关业务成本的数据,可以为讨论如何激励私人创新投资,同时确保患者和医疗体系的负担能力提供信息。

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