Biosimilar Uptake in Medicare Advantage vs Traditional Medicare

Author:

Kozlowski Steven1,Kwist Andrew2,McEvoy Rowan2,Koirala Nirabh2,Chillarige Yoganand2,Kelman Jeffrey A.3,Graham David J.1

Affiliation:

1. Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland

2. Acumen LLC, Burlingame, California

3. Centers for Medicare & Medicaid Services, Washington, DC

Abstract

This cross-sectional study uses Traditional Medicare and Medicare Advantage claims data to evaluate uptake of biosimilars relative to their reference products.

Publisher

American Medical Association (AMA)

Subject

Public Health, Environmental and Occupational Health,Health Policy

Reference6 articles.

1. Uptake and competition among biosimilar biological products in the US Medicare fee-for-service population.;Kozlowski;J Gen Intern Med,2022

2. Prescribing of low- versus high-cost Part B drugs in Medicare Advantage and traditional Medicare.;Anderson;Health Serv Res,2022

3. Ranibizumab and bevacizumab for neovascular age-related macular degeneration.;Martin;N Engl J Med,2011

4. Differences between managed care and fee-for-service Medicaid in the use of generics for high-rebate drugs: the cases of insulin glargine and glatiramer.;Hernandez;J Manag Care Spec Pharm,2020

5. USFDA. Purple Book: Lists of Licensed Biological Products With Reference Product Exclusivity and Biosimilarity or Interchangeability Evaluations. Accessed March 1, 2023. https://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/TherapeuticBiologicApplications/Biosimilars/ucm411418.htm

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