Kao-Ping Chua (
Lauren E. Kimmel is a law student at the University of Michigan School of Law. She was a research assistant in the Department of Pediatrics at the University of Michigan when this work was performed.
Health Aff (Millwood). 2021 Mar;40(3):453-460. doi: 10.1377/hlthaff.2020.01442.
The Orphan Drug Act of 1983 provides benefits to promote the development of treatments for rare diseases that have limited sales potential. Policy makers have questioned whether this purpose is furthered in the case of "partial orphan drugs" approved to treat both rare and common diseases, as many of these drugs are top sellers. In this study we used national commercial claims data to estimate the proportion of spending in the US on fifteen top-selling partial orphan drugs that was assigned to orphan indications in 2018. Of this spending, 21.4 percent was assigned to orphan indications, 70.7 percent to nonorphan indications, and 7.9 percent to neither orphan nor nonorphan indications (for example, off-label use). These findings support growing concerns regarding the costs of granting orphan drug benefits to the sponsors of top-selling partial orphan drugs.
1983 年的《孤儿药法案》为促进治疗罕见疾病的治疗方法的开发提供了益处,这些治疗方法的销售潜力有限。政策制定者质疑,在批准用于治疗罕见病和常见病的“部分孤儿药”的情况下,这一目的是否得到了进一步推进,因为许多此类药物都是畅销药。在这项研究中,我们使用国家商业索赔数据来估计 2018 年美国在 15 种畅销的部分孤儿药上的支出中,有多少被分配给孤儿适应症。在这部分支出中,21.4%被分配给孤儿适应症,70.7%被分配给非孤儿适应症,7.9%既不分配给孤儿适应症也不分配给非孤儿适应症(例如,标签外使用)。这些发现支持了人们对给予畅销部分孤儿药赞助商孤儿药福利的成本的日益关注。