Wyden Offers Support for Proposed Biosimilar Drug Payment Rule from CMS

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Wyden Offers Support for Proposed Biosimilar Drug Payment Rule from CMS

The following press release was published by the United States Senate Committee on Finance Chairman's News on Sept. 28, 2015. It is reproduced in full below.

WASHINGTON - Senate Finance Committee Ranking Member Ron Wyden, D-Ore., today sent a letter to the Centers for Medicare and Medicaid Services (CMS) offering support for their proposed rule on paying for biosimilar biological products (biosimilars):

“Biosimilar products should compete with one another - rather than set their own price - to ensure patients have access to affordable and high-quality drugs," Wyden said.

The Affordable Care Act (ACA) created a regulatory pathway for the Food and Drug Administration (FDA) to approve biological drugs that are determined to be “biosimilar" to, or “interchangeable" with, an FDA-licensed biological product. The ACA also contains a provision outlining a payment methodology for these products.

To implement this provision, CMS proposes to maintain a separate code for the reference biologic product and group the biosimilar products associated with that biologic into a single code. Each biosimilar associated with a single reference biologic drug will be paid based on the average sales price for all of the biosimilars in the code.

CMS’s proposal seeks to create a competitive environment amongst therapeutically equivalent products, which will have a real-time effect of driving down costs for patients and payers alike. With this proposal, biosimilar manufactures that produce lower-cost products will be more successful in securing greater market share than manufactures that produce higher-priced drugs, as they directly compete against one another.

The full letter can be found here.

Source: US Senate Committee on Finance Chairman's News

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