| Literature DB >> 31682491 |
Pinar Karaca-Mandic1, Jessica Chang2, Ronald Go3, Stephen Schondelmeyer4, Daniel Weisdorf5, Molly Moore Jeffery6.
Abstract
In 2015 the Food and Drug Administration approved filgrastim-sndz (Zarxio), the first US biosimilar. Following rapid uptake, by March 2018 filgrastim-sndz accounted for 47 percent of filgrastim administrations among commercially insured and 42 percent among Medicare Advantage beneficiaries. The initial cost difference between the originator and biosimilar was 31 percent in the former population but negligible in the latter.Keywords: Biologics; Biosimilar; Biosimilars; Cost reduction; FDA approvals process; Filgrastim-sndz; Health policy; Medicare Advantage; Out-of-pocket expenses; Pharmaceuticals; Prescription drug costs; Zarxio
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Year: 2019 PMID: 31682491 DOI: 10.1377/hlthaff.2019.00253
Source DB: PubMed Journal: Health Aff (Millwood) ISSN: 0278-2715 Impact factor: 6.301