CMS established a lower maximum copay for biosimilar and interchangeable biological products that is equivalent to the lower co-pay required for generic and preferred multiple source drugs.
In November 2017, the Centers for Medicare and Medicaid Services (CMS) released a proposed rule that included the proposal to lower cost sharing for and improve enrollee incentives to choose biosimilars over reference biologics, and to reduce costs to both Medicare Part D enrollees and the Part D program. This objective would have been accomplished by revising the definition of generic drug (§ 423.4) to include follow-on biologic products approved under the section 351(k) biosimilar pathway. This change would impact Low-Income Subsidy (LIS) cost sharing and non-LIS catastrophic coverage phase cost sharing, and would not be universally applied across other CMS policy.
In April 2018, CMS finalized the proposal to allow biosimilars to be covered at the generic copayment level for LIS-eligible beneficiaries and therefore achieve the intent of the original proposal. CMS did not revise the definition of generic drugs because their proposed approach "could be misinterpreted and create further confusion about the broader treatment of biosimilar and interchangeable biological products under the Part D program." But, instead, CMS established a lower maximum copay for biosimilar and interchangeable biological products that is equivalent to the lower co-pay required for generic and preferred multiple source drugs (revising § 423.782(a)(2)(iii)(A) and § 423.782(b)(3)) and will have the following impacts in 2019:
Institutionalized dual-eligible or receiving home- and community-based services:
Dual eligible, below or at 100% of the Federal Poverty Limit (FPL):
Dual eligible, above 100% FPL or Medicare-only below 135% FPL:
Medicare-only, between 135% and 150% FPL
The final rule did not change the cost sharing for biosimilar drugs to the same level as generic drugs for non-LIS beneficiaries in the catastrophic coverage phase. Under the new approach, the one that does not revise the definition of generic drug, CMS did not have the flexibility within statue to establish a lower copay.
The good news is that this change will not have a negative impact on non-LIS cost sharing in the catastrophic phase because such enrollees are required to pay cost sharing that is equal to the greater of the applicable copay amount ($3.40 for generic drugs or $8.50 for other products including biosimilars in 2019) or 5%. Given the high cost of biological products in general, the non-LIS catastrophic cost sharing will almost certainly be 5%.
The Top 5 Most-Read Biosimilar Articles of 2024
December 31st 2024The top 5 biosimilar-related articles of the year highlight a significant shift in the pharmaceutical industry, with projections indicating strong uptake in biosimilars at the expense of the originator products, despite challenges like uptake disparities and safety concerns.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
Top 5 Most-Read Rheumatology Articles of 2024
December 30th 2024The top 5 rheumatology biosimilar articles of 2024 highlight significant FDA approvals, including high-concentration adalimumab and tocilizumab biosimilars, along with evidence supporting the safety and efficacy of biosimilar-to-biosimilar switching.
Biosimilars Development Roundup for October 2024—Podcast Edition
November 3rd 2024On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, artificial intelligence (AI), and collaboration to enhance the global supply chain for biosimilars and generic drugs, as well as the evolving requirements for biosimilar devices.
The Top 5 Most-Read Policy Articles of 2024
December 28th 2024The top biosimilar policy articles of 2024 highlight advancements that include FDA guidance to simplify biosimilar interchangeability and CMS drug price negotiations under the Inflation Reduction Act, alongside challenges posed by pharmacy benefit manager rebate practices and the need for more active stakeholder engagement.
How Vertical Integration Drives Innovation and Access in Biosimilars
December 27th 2024Elie Bahou, PharmD, highlights how vertical integration in the biosimilar industry streamlines costs, improves supply reliability, accelerates market adoption, and enhances patient access, while emphasizing the value of collaboration, quality control, and value-based contracts for sustainable health care delivery.