US pharma giant Pfizer announced on 22 June 2017 that the US Food and Drug Administration (FDA) had rejected its application for approval of its epoetin alfa biosimilar.
FDA rejects Pfizer’s epoetin alfa biosimilar
Biosimilars/News | Posted 14/07/2017 0 Post your comment
The news comes less than a month after FDA advisers voted to recommend the approval of Pfizer’s biosimilar version of Amgen/Johnson & Johnson’s Epogen/Eprex/Procrit (epoetin alfa) [1].
Pfizer received a Complete Response Letter (CRL) regarding the company’s Biologics License Application (BLA) for its epoetin alfa biosimilar. The CRL was issued following manufacturing issues cited in a February FDA warning letter.
The warning letter was issued following a routine FDA inspection of a Hospira facility in McPherson, Kansas, USA in 2016, which listed significant good manufacturing practice (GMP) violations for finished pharmaceuticals. Although this facility was listed as the potential manufacturing site in the application for Pfizer’s epoetin alfa biosimilar, the company says that ‘the issues noted in the warning letter do not relate specifically to the manufacture of epoetin alfa’.
This is not the only rejection of a biosimilar application by FDA in the last year. The agency rejected Sandoz’s biosimilar pegfilgrastim application in July 2016 [2] and in June 2017 it rejected another pegfilgrastim biosimilar from Coherus [3].
Related articles
Sandoz withdraws biosimilar pegfilgrastim application
References
1. GaBI Online - Generics and Biosimilars Initiative. FDA advisors recommend approval of Pfizer’s epoetin alfa biosimilar [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Jul 7]. Available from: www.gabionline.net/Biosimilars/News/FDA-advisors-recommend-approval-of-Pfizer-s-epoetin-alfa-biosimilar
2. GaBI Online - Generics and Biosimilars Initiative. FDA rejects Sandoz’s biosimilar pegfilgrastim application [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Jul 7]. Available from: www.gabionline.net/Biosimilars/News/FDA-rejects-Sandoz-s-biosimilar-pegfilgrastim-application
3. GaBI Online - Generics and Biosimilars Initiative. FDA rejects pegfilgratim biosimilar from Coherus [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Jul 7]. Available from: insert once uploaded = www.gabionline.net/Biosimilars/News/FDA-rejects-pegfilgrastim-biosimilar-from-Coherus
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2017 Pro Pharma Communications International. All Rights Reserved.
Source: Pfizer
Research
Long-term real-world safety experience of biosimilars confirms concept of biosimilarity
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
General
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
SBR issues consensus on interchangeability of reference products and biosimilars
Comments (0)
Post your comment