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WASHINGTON, Sept. 11, 2017 /PRNewswire-USNewswire/ -- Today, the Biologics Prescribers Collaborative (BPC) and five other groups representing a broad spectrum of physicians who prescribe biologics, urged the U.S. Centers for Medicare and Medicaid Services (CMS) to revise their current payment policy for biosimilars by adopting unique Healthcare Common Procedure Coding System (HCPCS) billing codes otherwise known as J-codes.
The six groups call for CMS to not take a generic approach for biosimilars medicines that are, according to scientific fact, not identical to their reference products as generics are. The groups – Alliance for Patient Access, American Association of Clinical Endocrinologists, American College of Rheumatology, American Gastroenterological Association, Biologics Prescribers Collaborative and the Coalition of State Rheumatology Organizations – support CMS' intent to create competition in the market, but believe that different reimbursement levels for different biosimilars will go beyond promoting competition and will help to create a more robust market while protecting patient safety.
BPC's comment encourages CMS to consider for the following reasons:
"The current reimbursement landscape is extremely complex. Unique J-codes for biosimilars help clarify for physicians that while 'highly similar,' biosimilars of the same reference product will likely still have product differences that should be considered in clinical decision-making," said BPC co-convener Dr. Dennis Cryer. "Grouping biosimilars in one blended reimbursement rate prioritizes price above all other features and has the potential to undermine patient care and safety."
The groups appreciate CMS requesting additional stakeholder comments on this important issue and BPC looks forward to the greater availability of biosimilars which have the potential to improve access and increase therapeutic options for patients.
The Biologics Prescribers Collaborative is an organization of groups representing physicians who regularly prescribe biologics that aims to ensure that sound policies are in place to promote the safest possible use of all biologics, including biosimilars, for all patients.
The comment can be found below.
Comment on CMS-1676-P Medicare Program: Revisions to Payment Policies Under Physician Fee Schedule and Other Revisions to Part B for CY 2018; Medicare Shared Savings Program Requirements; and Medicare Diabetes Prevention Program – Section D: Payment for Biosimilar Biological Products under Section 1847A of the Act
September 11, 2017
Seema Verma, Administrator
Centers for Medicare and Medicaid Services
Department of Health and Human Services
Hubert H. Humphrey Building, Room 445-G
200 Independence Avenue, SW
Washington, D.C. 20201
Dear Administrator Verma:
As physicians who routinely prescribe biologic medicines and on behalf of professional organizations with numerous biologics prescribers as members, we appreciate the opportunity to provide additional perspective on Healthcare Common Procedure Coding System (HCPCS) billing codes (J-codes) for biosimilar medicines.
We hold that unless a biosimilar is deemed by the FDA to be "interchangeable" with the reference biologic, each biosimilar should have a unique J-code, for the following reasons:
Biosimilars can only be similar to their reference product, not identical like a small-molecule generic drug. Biosimilars, like all biologics, are large molecules grown in living systems. Assigning one reimbursement code for all biosimilars of the same reference product follows the generics reimbursement policy and ignores the fundamental science.
One reimbursement rate makes no provision for the approval of interchangeable biosimilars. In fact, such a policy seems to treat all biosimilars for a given reference product as interchangeable. Determinations of interchangeability must be made by FDA and based solely on scientific and medical considerations. Interchangeability requires a higher level of evidence than biosimilarity.
For any given innovative biologic, physicians will have many different biosimilars from which to choose and will seek to prescribe the right biosimilar for patients based on clinical appropriateness. Having multiple treatment options allows physicians the ability to provide individualized care. For example, there are currently two biosimilars – Inflectra and Renflexis – for the branded biologic Remicade and potentially five more in development. If the biosimilar's list price is greater than the blended ASP, physicians could experience reimbursement losses and as such there will be instances where prescribers face financial barriers to choosing the most appropriate biosimilar medicine.
Despite important differences between biosimilar medicines, hospitals and payers could mandate use of the lowest cost biosimilar at any given time, reducing choice and potentially encouraging inappropriate non-medical switching back and forth between one biologic/biosimilar and another. Non-medical switching can only be justified if the FDA has determined interchangeability between the biosimilar and the reference biologic.
Currently, CMS prioritizes price over all other product features, which could deter innovation and may discourage manufacturers from investing in research to gain approval for all indications. Access to a choice of biosimilars is important for our patients, especially where an individual patient's immune reaction may differ between drugs.
Price differentiation reflects that while "highly similar," different biosimilars of the same reference product may still have important product differences, such as:
Manufacturers must be properly incentivized to develop innovative biosimilar products or the market will fail to prosper, which could lead to fewer treatment options and undermine the promise and purpose of the entire class of biosimilar products.
In closing, BPC believes in the promise of a biosimilars market that will yield important benefits for patients who suffer from chronic, life threatening illnesses. Biologics have revolutionized the treatment of many different cancers, autoimmune diseases and blood disorders. Biosimilars will create greater access and more therapeutic options for these patients.
We urge CMS to rethink its payment policy for biosimilars and not take a generic approach for medicines that are, by definition, not generic. BPC supports CMS' intent to create competition in the market, but believes that different reimbursement levels for different biosimilars will go further to promote competition, create a robust market, and protect patient safety. Thank you for your consideration of the prescribers' perspective as you make these important payment determinations.
Alliance for Patient AccessAmerican Association of Clinical EndocrinologistsAmerican College of RheumatologyAmerican Gastroenterological AssociationBiologics Prescribers CollaborativeCoalition of State Rheumatology Organizations
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