Biosimilar Uptake in Medicare Advantage vs Traditional Medicare
Author:
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
Publisher
American Medical Association (AMA)
Subject
Public Health, Environmental and Occupational Health,Health Policy
Link
https://jamanetwork.com/journals/jama-health-forum/articlepdf/2813299/kozlowski_2023_ld_230036_1702577727.30785.pdf
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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