拟议的价格法规对加拿大新专利药品上市的影响:一项回顾性队列研究。

IF 9.4 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Canadian Medical Association journal Pub Date : 2024-05-26 DOI:10.1503/cmaj.231485
Wei Zhang, Huiying Sun, Daphne P Guh, Paul Grootendorst, Aidan Hollis, Aslam H Anis
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引用次数: 0

摘要

背景:专利药品价格审查委员会(PMPRB)是加拿大专利药品价格的监管机构,于 2017 年 12 月发布了监管框架的拟议修正案。由于一系列修改和延迟,修订后的政策尚未最终确定。我们试图评估 PMPRB 政策的不确定性对专利药上市的潜在早期影响:我们根据 IQVIA MIDAS 数据库 2012-2021 年的销售数据,对在加拿大和 13 个国家销售的专利药品(分子)建立了一个回顾性队列,这些国家是 PMPRB 目前使用或建议用作价格比较对象的国家。结果是分子是否在全球首次上市(2 年上市)后 2 年内在特定国家上市(即销售)。我们分别采用间断时间序列和逻辑回归的方法,比较了加拿大在拟议修正案公布前(2012-2017 年)和公布后("不确定期",2018-2021 年)的 2 年上市变化情况,以及美国和其他 12 个国家组("其他国家组")的变化情况。我们还对每个国家进行了分析,并按分子特征(如治疗效果)分别进行了分组分析:我们分别纳入了 242 种和 107 种在拟议修正案公布前和不确定期间上市的新分子。相应的两年上市比例分别为:加拿大 45.0% 和 30.8%,美国 81.4% 和 82.2%,其他国家组 83.9% 和 70.1%。所有分析均显示,在不确定期间,美国和其他国家组的 2 年投放量变化与加拿大的变化相似。挪威和瑞典的下降幅度大于加拿大。在不确定期间,加拿大具有主要治疗效果的分子的 2 年上市比例从 45.8%下降到 31.3%,其他国家组从 87.5%下降到 62.5%,但美国从 91.7%上升到 100%:加拿大与价格参照国相比,除了具有重大治疗效果的分子药物外,PMPRB 政策的不确定性对分子药物的上市没有负面影响。加拿大具有重大治疗效果的药物上市量减少的情况需要继续调查。
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The impact of proposed price regulations on new patented medicine launches in Canada: a retrospective cohort study.

Background: The Patented Medicine Prices Review Board (PMPRB), the agency that regulates the prices of patented medicines in Canada, published proposed amendments to the regulatory framework in December 2017. Because of a series of changes and delays, the revised policy has not yet been finalized. We sought to evaluate the potential early impact of the uncertainty about the PMPRB policy on patented-medicine launches.

Methods: We developed a retrospective cohort of patented medicines (molecules) sold in Canada and the 13 countries that the PMPRB currently uses or has proposed to use as price comparators, from sales data from the IQVIA MIDAS database for 2012-2021. The outcome was whether a molecule was launched (i.e., sold) in a specific country within 2 years of its global first launch (2-yr launch). We compared the change of 2-year launch before (2012-2017) and after the proposed amendments were published ("uncertain period," 2018-2021) in Canada with the change in the United States and the other 12 countries as a group ("other-countries group"), using interrupted time series and logistic regressions, respectively. We further conducted analyses for each individual country and subgroups by molecule characteristics, such as therapeutic benefit, separately.

Results: We included 242 and 107 new molecules launched before publication of the proposed amendments and during the uncertain period, respectively. The corresponding 2-year launch proportions were 45.0% and 30.8% in Canada, 81.4% and 82.2% in the US, and 83.9% and 70.1% in the other-countries group. All analyses showed changes in 2-year launch during the uncertain period in the US and in the other-countries group that were similar to the changes in Canada. Greater decreases were observed in Norway and Sweden than in Canada. The 2-year launch proportion for molecules with major therapeutic benefit decreased from 45.8% to 31.3% in Canada during the uncertain period and from 87.5% to 62.5% in the other-countries group, but increased from 91.7% to 100% in the US.

Interpretation: No negative impact of the PMPRB-policy uncertainty on molecule launches was observed when comparing Canada with price-comparator countries, except for molecules with major therapeutic benefit. The reduction in launches of medicines with major therapeutic benefit in Canada requires continuing investigation.

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来源期刊
Canadian Medical Association journal
Canadian Medical Association journal 医学-医学:内科
CiteScore
8.30
自引率
4.10%
发文量
481
审稿时长
4-8 weeks
期刊介绍: CMAJ (Canadian Medical Association Journal) is a peer-reviewed general medical journal renowned for publishing original research, commentaries, analyses, reviews, clinical practice updates, and editorials. Led by Editor-in-Chief Dr. Kirsten Patrick, it has a significant impact on healthcare in Canada and globally, with a 2022 impact factor of 17.4. Its mission is to promote knowledge vital for the health of Canadians and the global community, guided by values of service, evidence, and integrity. The journal's vision emphasizes the importance of the best evidence, practice, and health outcomes. CMAJ covers a broad range of topics, focusing on contributing to the evidence base, influencing clinical practice, and raising awareness of pressing health issues among policymakers and the public. Since 2020, with the appointment of a Lead of Patient Involvement, CMAJ is committed to integrating patients into its governance and operations, encouraging their content submissions.
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