Drugs anticipated to be selected for the Medicare Drug Price Negotiation Program in 2025.

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Emma M Cousin, Sean D Sullivan, Ryan N Hansen, Nico Gabriel, Ayuri S Kirihennedige, Inmaculada Hernandez
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引用次数: 0

Abstract

Background: The Centers for Medicare and Medicaid Services (CMS) recently announced the Maximum Fair Price for the first 10 Medicare Part D drugs selected for price negotiation. By February 2025, CMS should announce the list of Part D drugs to be negotiated with implementation of the negotiated prices in 2027.

Objective: To identify up to 15 Medicare Part D single-source drugs anticipated to be selected by CMS for price negotiation in 2025.

Methods: We followed selection criteria identified in the Inflation Reduction Act and CMS guidance to identify drugs. We projected 2023 Part D gross spending using 2020-2022 data reported by CMS and linear prediction models. We ranked products according to the projected spending figure and identified those not eligible for selection because of (1) number of years since approval, (2) availability of a biosimilar or generic version, (3) approval for a single orphan indication, (4) whole human blood or plasma-derived, or (5) eligibility for the small biotech exception.

Results: We identified 13 products likely subject to Medicare drug price negotiation, including 4 anticancer therapies, 3 noninsulin antidiabetic products, 2 inhalers, 1 antifibrotic therapy, 1 gastrointestinal agent, 1 enzyme replacement therapy, and 1 product indicated for dyskinesia. These 13 products each had projected annual gross Part D spending more than $1 billion. We identified 7 additional products with uncertainty to complete the list of 15, including an insulin, an antiviral, an antibiotic, an immunologic agent, an antidiabetic, and 2 cancer drugs. These products had projected gross Part D spending between $877 million and $1.399 billion. Twenty-two products with comparable levels of spending were deemed ineligible for selection because of availability of a generic or biosimilar version (10 products), insufficient years since approval (8 products), eligibility for the small biotech exception (3 products), and expected market discontinuation (1 product).

Conclusions: Our identification of products anticipated to be selected for negotiation in 2025 (with implementation of negotiated prices in 2027) will help inform manufacturers, payers, patients, and policymakers of the products that will likely see a decrease in Medicare drug prices as result of negotiation. We identified 22 products with levels of spending that are comparable with those anticipated to be selected for negotiation but are not eligible, primarily because of generic or biosimilar availability or insufficient time on market.

预计 2025 年将被选入医疗保险药品价格谈判计划的药品。
背景:医疗保险和医疗补助服务中心(CMS)最近公布了首批 10 种选定进行价格谈判的医疗保险 D 部分药物的最高公平价格。到 2025 年 2 月,CMS 将公布 D 部分药品谈判清单,并于 2027 年执行谈判价格:目标:确定预计将由 CMS 在 2025 年选择进行价格谈判的多达 15 种医疗保险 D 部分单一来源药物:我们遵循《通货膨胀削减法》和 CMS 指南中确定的选择标准来确定药物。我们使用 CMS 报告的 2020-2022 年数据和线性预测模型预测了 2023 年 D 部分的总支出。我们根据预测的支出数字对产品进行了排序,并确定了因以下原因而不符合选择条件的产品:(1)批准后的年限;(2)生物类似药或仿制药的可用性;(3)批准用于单一孤儿适应症;(4)源自全人类血液或血浆;或(5)符合小型生物技术例外情况:我们确定了 13 种可能需要进行医疗保险药品价格谈判的产品,包括 4 种抗癌疗法、3 种非胰岛素抗糖尿病产品、2 种吸入剂、1 种抗纤维化疗法、1 种胃肠道药物、1 种酶替代疗法和 1 种用于运动障碍的产品。这 13 种产品的 D 部分预计年度总支出均超过 10 亿美元。我们又确定了 7 种具有不确定性的产品,以完成 15 种产品的清单,包括 1 种胰岛素、1 种抗病毒药、1 种抗生素、1 种免疫制剂、1 种抗糖尿病药和 2 种抗癌药。这些产品的 D 部分预计总支出在 8.77 亿美元至 13.99 亿美元之间。有 22 种支出水平相当的产品被认为不符合入选条件,原因是已有非专利药或生物类似药(10 种产品)、获批时间不足(8 种产品)、符合小型生物技术例外情况(3 种产品)以及预计市场停产(1 种产品):我们对预计在 2025 年(2027 年实施谈判价格)被选中进行谈判的产品进行了鉴定,这将有助于制造商、付款人、患者和政策制定者了解因谈判而可能降低医疗保险药品价格的产品。我们发现有 22 种产品的支出水平与预计将被选中进行谈判的产品相当,但不符合条件,主要原因是仿制药或生物类似药的可用性或上市时间不足。
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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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