Estimating Costs of Market Exclusivity Extensions For 4 Top-Selling Prescription Drugs in the US.

IF 11.3 Q1 HEALTH CARE SCIENCES & SERVICES
Dongzhe Hong, S Sean Tu, Reed F Beall, Massimiliano Russo, Benjamin N Rome, Aaron S Kesselheim, Ameet Sarpatwari
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引用次数: 0

Abstract

Importance: Brand-name drugs in the US are sold at high prices during market exclusivity periods defined by their patents, before prices are lowered by generic competition. Drug manufacturers use several strategies to extend these market exclusivity periods and delay generic competition, including obtaining overlapping thickets of patents.

Objective: To estimate excess US spending associated with delays in generic competition due to extended market exclusivity for 4 top-selling drugs.

Design, setting, and participants: This retrospective serial cross-sectional study focused on 4 top-selling drugs that experienced new generic competition between 2014 and 2018 to allow enough time for determining postexclusivity price trajectories: imatinib (Gleevec, cancer), glatiramer (Copaxone, multiple sclerosis), celecoxib (Celebrex, arthritis), and bimatoprost (Lumigan, glaucoma). Drug monthly spending data from 2011 to 2021 were retrieved from a large commercial claims database (Merative MarketScan) and a random sample of Medicare beneficiaries with at least 1 month of Medicare Parts A, B, and D coverage and adjusted for estimated rebates obtained from SSR Health, LLC. The analysis was performed between March 2023 and January 2024.

Exposures: Extended market exclusivity was calculated as the time between expiration of the key patent and first generic marketing.

Main outcomes and measures: The primary outcome was net monthly national drug spending in commercial insurance and Medicare Part D. Spending was estimated under 2 scenarios: (1) the status quo, reflecting observed spending trends, and (2) a counterfactual scenario, modeling spending in the absence of extended market exclusivity. Segmented linear regression analyses were used to assess level and slope changes in monthly spending following generic entry. Weights were applied to extrapolate sample-based estimates to the full US commercially insured and Medicare Part D populations.

Results: Market exclusivity extensions beyond expiration of the key patent ranged from 7 (celecoxib) to 13 (glatiramer) months. In the absence of extended market exclusivity, and over a 2-year period following generic competition, net spending would have decreased by $3.5 billion, including $1.9 (95% CI, $1.3-$2.5) billion in commercial plans and $1.6 (95% CI, $1.1-$2.1) billion in Medicare-including $67 (95% CI, $22-$115) million for bimatoprost, $726 (95% CI, $516-$938) million for celecoxib, $1.7 (95% CI, $1.0-$2.4) billion for glatiramer, and $1.0 (95% CI, $0.8-$1.2) billion for imatinib.

Conclusions and relevance: This study found that promoting timely generic availability and avoiding extending market exclusivity for top-selling drugs may result in substantial savings for US patients and payers, including both public and private health insurance programs.

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估算美国4种最畅销处方药的市场独占性延长成本。
重要性:在美国,品牌药在其专利规定的市场独占期以高价出售,然后在仿制药竞争中降价。药品制造商使用几种策略来延长这些市场独占期和延迟仿制药竞争,包括获得重叠的专利丛。目的:估计由于4种最畅销药物的市场专有权延长而导致的仿制药竞争延迟相关的美国超额支出。设计、环境和参与者:本回顾性系列横贯研究集中于2014年至2018年期间经历了新的仿制药竞争的4种畅销药物,以便有足够的时间确定独占后的价格轨迹:伊马替尼(格列卫,癌症)、格拉替默(科帕松,多发性硬化症)、塞来昔布(西乐葆,关节炎)和比马前列素(鲁米根,青光眼)。从大型商业索赔数据库(Merative MarketScan)和至少有1个月医疗保险a、B和D部分覆盖的医疗保险受益人随机样本中检索2011年至2021年的药品月度支出数据,并根据SSR Health, LLC获得的估计回扣进行调整。分析于2023年3月至2024年1月进行。风险:延长的市场独占性计算为关键专利到期和首次仿制药上市之间的时间。主要结果和措施:主要结果是商业保险和医疗保险d部分每月全国药品净支出,支出在两种情况下进行估计:(1)现状,反映观察到的支出趋势;(2)反事实情景,模拟没有扩展市场排他性的支出。分段线性回归分析用于评估通用条目后每月支出的水平和斜率变化。权重应用于外推基于样本的估计,以美国全部商业保险和医疗保险D部分人口。结果:关键专利到期后的市场独占延长时间从7个月(塞来昔布)到13个月(格拉替默)不等。在没有延长市场独占权的情况下,在仿制药竞争后的2年期间,净支出将减少35亿美元,其中包括19亿美元(95% CI, 13 - 25亿美元)用于商业计划,16亿美元(95% CI, 11 - 21亿美元)用于医疗保险,包括67亿美元(95% CI, 22- 1.15亿美元)用于比马托前列,726亿美元(95% CI, 5.16 - 9.38亿美元)用于塞来昔布,17亿美元(95% CI, 10 - 24亿美元)用于格拉替默,1.0亿美元(95% CI, 8- 12亿美元)用于伊马替尼。结论和相关性:本研究发现,促进及时获得仿制药,避免扩大畅销药物的市场独占性,可能会为美国患者和支付款人(包括公共和私人医疗保险计划)节省大量资金。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
7.80%
发文量
0
期刊介绍: JAMA Health Forum is an international, peer-reviewed, online, open access journal that addresses health policy and strategies affecting medicine, health, and health care. The journal publishes original research, evidence-based reports, and opinion about national and global health policy. It covers innovative approaches to health care delivery and health care economics, access, quality, safety, equity, and reform. In addition to publishing articles, JAMA Health Forum also features commentary from health policy leaders on the JAMA Forum. It covers news briefs on major reports released by government agencies, foundations, health policy think tanks, and other policy-focused organizations. JAMA Health Forum is a member of the JAMA Network, which is a consortium of peer-reviewed, general medical and specialty publications. The journal presents curated health policy content from across the JAMA Network, including journals such as JAMA and JAMA Internal Medicine.
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