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《降低通胀法案》与药物研发:对批准后临床试验影响的潜在早期信号

The Inflation Reduction Act and Drug Development: Potential Early Signals of Impact on Post-Approval Clinical Trials.

作者信息

Zheng Hanke, Patterson Julie A, Campbell Jonathan D

机构信息

National Pharmaceutical Council, Washington, DC, USA.

出版信息

Ther Innov Regul Sci. 2025 Apr 22. doi: 10.1007/s43441-025-00774-2.

Abstract

BACKGROUND

The Inflation Reduction Act's (IRA) Drug Price Negotiation Program (DPNP) may reduce incentives for industry investments in post-approval clinical development. We aimed to explore the IRA's impact on the initiation of industry-sponsored, post-approval clinical trials.

METHODS

Using Citeline's Trialtrove database (7/2014-8/2024), we conducted an interrupted time series analysis (ITSA) to estimate the IRA's impact on the initiation of industry-sponsored Phase I-III trials in previously approved drugs, excluding all vaccines and COVID-19 treatments. We conducted an additional ITSA to examine post-IRA changes in government-funded trials, hypothesized to be unaffected by the IRA, and sensitivity analyses to explore potential exogenous confounding factors. Finally, we explored differences in the IRA's impact on post-approval industry-sponsored clinical trial initiation in small versus large molecule drugs.

RESULTS

Following the IRA's passage, the average monthly number of industry-sponsored trials on post-approval drugs decreased by 38.4%. The ITSA indicated that the IRA's passage was associated with an immediate drop of 11.1 industry-sponsored trials (p-value < 0.05) and an additional decrease by 0.9 trials per month (p-value < 0.01). The IRA's passage was not statistically associated with changes in government-funded trial initiation. Sensitivity analyses supported ITSA findings. Initiation of post-approval industry-sponsored trials decreased by 47.3% and 32.9% for small and large molecule drugs, respectively.

CONCLUSIONS

The IRA's passage was associated with reductions in industry-sponsored, but not government-funded, post-approval trials, with larger reductions for small molecule drugs. These findings provide early evidence supporting concerns around IRA-related reductions in incentives for post-approval clinical development.

摘要

背景

《降低通胀法案》(IRA)的药品价格谈判计划(DPNP)可能会降低行业对批准后临床开发的投资积极性。我们旨在探讨IRA对行业赞助的批准后临床试验启动的影响。

方法

利用Citeline的Trialtrove数据库(2014年7月至2024年8月),我们进行了中断时间序列分析(ITSA),以估计IRA对先前批准药物中行业赞助的I-III期试验启动的影响,不包括所有疫苗和新冠治疗药物。我们进行了另一项ITSA,以研究政府资助试验在IRA通过后的变化(假设不受IRA影响),并进行敏感性分析以探索潜在的外源性混杂因素。最后,我们探讨了IRA对小分子药物和大分子药物批准后行业赞助临床试验启动影响的差异。

结果

IRA通过后,行业赞助的批准后药物试验的平均月数量下降了38.4%。ITSA表明,IRA的通过与行业赞助试验立即减少11.1项相关(p值<0.05),且每月额外减少0.9项试验(p值<0.01)。IRA的通过与政府资助试验启动的变化无统计学关联。敏感性分析支持了ITSA的结果。小分子药物和大分子药物批准后行业赞助试验的启动分别下降了47.3%和32.9%。

结论

IRA的通过与行业赞助的批准后试验减少有关,但与政府资助的试验无关,小分子药物的减少幅度更大。这些发现提供了早期证据,支持了对IRA相关的批准后临床开发激励措施减少的担忧。

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