考虑到大型和小型生物制药公司的不同贡献,建立降低通货膨胀率的价格谈判对新药研发管线的影响模型。

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Gregory Vaughan, Roger Du, Fred D Ledley
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引用次数: 0

摘要

背景/目的:通货膨胀削减法》中规定由医疗保险与医疗补助服务中心进行药品价格谈判,这一条款被批评为对医药创新的威胁。本研究根据大型制药公司和小型生物技术公司对临床试验的不同贡献以及资金供应情况,模拟了《通胀削减法》对药品审批的潜在影响:本研究考察了上市生物制药公司的研发费用、收入和新投资(普通股和优先股的出售),以及对 ClinicalTrials.gov 中分阶段临床试验的赞助情况。财务数据被纳入一个模型中,该模型根据报告的特定阶段成本和过渡率、不同规模公司的试验赞助比例、基于公司规模的研发支出预计减少量以及大公司可能在临床阶段之间分配研发支出减少量的三种情况来估算每个阶段的药物数量和批准量:(1)各阶段的研发支出按比例减少;(2)2-3 阶段的研发支出按比例减少;(3)1-2 阶段的研发支出按比例减少:研究了 1378 家上市生物制药公司(2000-2018 年)的财务数据。79家市值≥70亿美元的大型公司的研发费用与收入相关,收入减少10%,研发费用减少8.4%。对于 1299 家市值较小的公司,结论是:研发费用与收入相关:这项研究表明,《通货膨胀削减法》中的药品价格谈判条款对药品批准数量的影响很小,甚至没有影响。虽然大型制药公司可能会减少研发支出,但小型公司的持续研发以及大型公司对研发资源的战略性分配可能会减轻《通胀抑制法案》的负面影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modeling impact of inflation reduction act price negotiations on new drug pipeline considering differential contributions of large and small biopharmaceutical companies.

Background/aims: Provisions of the Inflation Reduction Act mandating drug price negotiation by the Centers for Medicare & Medicaid Services have been criticized as a threat to pharmaceutical innovation. This study models potential impacts of the Inflation Reduction Act on drug approvals based on the differential contributions of large pharmaceutical companies and smaller biotechnology firms to clinical trials and the availability of capital.

Methods: This study examined research and development expense, revenue, and new investment (sale of common and preferred stock) by public biopharmaceutical companies and sponsorship of phased clinical trials in ClinicalTrials.gov. Financial data were incorporated in a model that estimates the number of drugs in each phase and approvals from reported phase-specific costs and transition rates, proportional sponsorship of trials by companies of different size, projected reductions in research and development spending based on company size, and three scenarios by which large companies may allocate reductions in research and development spending among clinical phases: (1) research and development proportionally reduced across phases; (2) research and development disproportionally reduced in phases 2-3; and (3) research and development disproportionately reduced in phases 1-2.

Results: Financial data were examined for 1378 public biopharmaceutical companies (2000-2018). Research and development expense was associated with revenue for 79 large companies with market capitalization ≥$7 billion with a 10% reduction in revenue reducing research and development expense by 8.4%. For 1299 smaller companies with market capitalization <$7 billion, research and development was associated with new investment, but not revenue. Smaller companies sponsored 55.2% of phase 1, 55.6% of phase 2, and 49.8% of phase 3 trials in ClinicalTrials.gov 2013-2018. In a model of clinical development that apportions clinical trials between large and smaller companies and determines the number of trials based on research and development resources, 400 drugs entering development produced 47.3 approvals (11.83% rate). A 10% reduction in revenue, reflecting the upper boundary of observed changes 2000-2018, with (1) proportional reduction across phases 1-3 produced 45.1 approvals (4.61% reduction); (2) disproportional reduction of phases 2-3 produced 42.8 approvals (9.55% reduction); and (3) disproportional reduction of phases 1-2 produced 46.9 approvals (0.95% reduction).

Conclusion: This work suggests that the drug price negotiation provisions of the Inflation Reduction Act could have little or no impact on the number of drug approvals. While large pharmaceutical companies may reduce research and development spending, continued research and development by smaller companies and strategic allocation of research and development resources by large companies may mitigate any negative effects of the Inflation Reduction Act.

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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
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