Uptake of the Biologic Filgrastim and Its Biosimilar Product Among the Medicare Population

Author:

Kozlowski Steven1,Birger Noy2,Brereton Stephaeno2,McKean Stephen J.2,Wernecke Michael2,Christl Leah1,Kelman Jeffrey A.3

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

Publisher

American Medical Association (AMA)

Subject

General Medicine

Reference6 articles.

1. Biosimilars and the European experience: implications for the United States.;Megerlin;Health Aff (Millwood),2013

2. Biosimilar competition: lessons from Europe.;Grabowski;Nat Rev Drug Discov,2014

3. US Food and Drug Administration. Center for Drug Evaluation and Research list of licensed biological products. https://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/TherapeuticBiologicApplications/Biosimilars/UCM560162.pdf. Accessed June 4, 2018.

4. RoyzmanI. United States: the value of being highly similar: first US biosimilar. http://www.mondaq.com/unitedstates/x/391742/food+drugs+law/The+Value+of+Being+Highly+Similar+First+US+Biosimilar. Accessed February 18, 2018.

5. FDANews. Sandoz launches Zarxio at 15 percent lower price than Neupogen. https://www.fdanews.com/articles/173036-sandoz-launches-zarxio-at-15-percent-lower-price-than-neupogen. Accessed February 18, 2018.

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