John F. Kennedy School of Government, Harvard University, Cambridge, Massachusetts.
Harvard Business School, Boston, Massachusetts.
JAMA Intern Med. 2024 Jan 1;184(1):63-69. doi: 10.1001/jamainternmed.2023.6293.
The Inflation Reduction Act (IRA) requires Medicare to negotiate prices for some high-spending drugs but exempts drugs approved solely for the treatment of a single rare disease.
To estimate Medicare spending and global revenues for drugs that might have been exempt from negotiation from 2012 to 2021.
DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study analyzed drugs that met the IRA threshold for price negotiation (Medicare spending >$200 million/y) in any year from 2012 to 2021 and had an Orphan Drug Act designation. We stratified drugs into 4 mutually exclusive categories: approved for a single rare disease (sole orphan), approved for multiple rare diseases (multiorphan), initially approved for a rare disease and subsequently approved for a nonrare disease (orphan first), and initially approved for a nonrare disease and subsequently approved for a rare disease (non-orphan first).
The primary outcomes were the number of sole orphan drugs, estimated Medicare spending on those drugs from 2012 to 2021, and global revenue since launch.
Among 282 drugs, 95 (34%) were approved to treat at least 1 rare disease, including 25 sole orphan drugs (26%), 20 multiorphan drugs (21%), 13 orphan first drugs (14%), and 37 non-orphan first drugs (39%). From 2012 to 2021, Medicare spending on sole orphan drugs increased from $3.4 billion to $10.0 billion. Each year, a median (IQR) of $2.5 ($1.9-$2.6) billion in Medicare spending would have been excluded from price negotiation because of the sole orphan exemption. The cumulative global revenue of the median (IQR) sole orphan drug was $11 ($6.6-$19.2) billion.
The sole orphan exemption will exclude billions of dollars of Medicare drug spending from price negotiation. The high level of global revenues achieved by these drugs, however, suggests that special exemption is unnecessary for them to achieve financial success. Congress could consider removing the sole orphan exemption to obtain additional savings for patients and taxpayers and to eliminate any potential disincentive for developing additional indications for these drugs.
《降低通胀法案》(IRA)要求医疗保险对一些高支出药物进行谈判,但豁免了仅用于治疗单一罕见疾病的药物。
估计从 2012 年到 2021 年,可能免于谈判的药物的医疗保险支出和全球收入。
设计、设置和参与者:本横断面研究分析了在 2012 年至 2021 年的任何一年中符合 IRA 价格谈判门槛(医疗保险支出> 2 亿美元/年)且具有孤儿药法案指定的药物。我们将药物分为 4 个互斥类别:批准用于单一罕见疾病(单一孤儿)、批准用于多种罕见疾病(多孤儿)、最初批准用于罕见疾病随后批准用于非罕见疾病(孤儿第一)和最初批准用于非罕见疾病随后批准用于罕见疾病(非孤儿第一)。
主要结果是单一孤儿药物的数量、2012 年至 2021 年期间这些药物的医疗保险支出估计数以及上市以来的全球收入。
在 282 种药物中,有 95 种(34%)被批准用于治疗至少 1 种罕见疾病,包括 25 种单一孤儿药物(26%)、20 种多孤儿药物(21%)、13 种孤儿第一药物(14%)和 37 种非孤儿第一药物(39%)。从 2012 年到 2021 年,医疗保险对单一孤儿药物的支出从 34 亿美元增加到 100 亿美元。由于单一孤儿豁免,每年医疗保险支出中都会有中位数(IQR)250 亿美元(190-260 亿美元)被排除在价格谈判之外。中位数(IQR)单一孤儿药物的全球累计收入为 110 亿美元(66-192 亿美元)。
单一孤儿豁免将使医疗保险药物支出的数十亿美元免于价格谈判。然而,这些药物实现的高全球收入表明,对它们来说,特殊豁免对于实现财务成功是不必要的。国会可以考虑取消单一孤儿豁免,为患者和纳税人节省更多费用,并消除开发这些药物的其他适应症的任何潜在障碍。