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Pegfilgrastim Biosimilars: Where Are We Now?

In 1991, the U.S. Food & Drug Administration (FDA) approved rmetHuGCSF for human use. This recombinant methionyl human granulocyte colony-stimulating factor, or filgrastim, saw use in over 1 million patients in its first 5 years on the market. In 2002, the FDA approved a version of filgrastim wi...

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Bibliografske podrobnosti
izdano v:J Adv Pract Oncol
Main Authors: Selby, Christopher, Peyton-thomas, Breanne, Eslami, Parnian
Format: Artigo
Jezik:Inglês
Izdano: Harborside Press LLC 2021
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8299796/
https://ncbi.nlm.nih.gov/pubmed/34430064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6004/jadpro.2021.12.5.9
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