Biocon/Mylan’s biosimilar programme has hit a stumbling block after failing an inspection by the French inspecting authority (L’Agence nationale de sécurité du médicament et des produits de santé: ANSM).
Setback in Biocon/Mylan’s biosimilar programme after GMP inspection
Biosimilars/General
|
Posted 11/08/2017
0
Post your comment

India-based biologicals specialist Biocon announced on 9 July 2017 that, although it had received good manufacturing practice (GMP) approval for ‘Biologics Drug Substance facilities’ from ANSM, its ‘Drug Product facility’ would have to be reinspected.
The inspection was carried out at its Bangalore drug substance and drug product sites, where ANSM found issues with its product plant. Biocon said that although there were ‘no critical observations’, the site will require a follow-up inspection to verify that Biocon has implemented the ‘proposed corrective and preventive actions (CAPAs)’ before it will gain a GMP compliance certificate for its drug product facility.
The decision affects the pending European Medicines Agency (EMA) Marketing Authorization Applications for trastuzumab, pegfilgrastim and insulin glargine (pen assembly only). Biocon/Mylan submitted their application for their pegfilgrastim biosimilar to EMA for approval in July 2016 [1]. The application for their trastuzumab biosimilar was submitted to EMA in August 2016 [2]. The application for their insulin glargine biosimilar was submitted to EMA in November 2016 [3].
Biocon said that the ANSM has ‘reviewed the proposed CAPA plan’ and that it ‘is progressing towards completion of the implementation of these CAPAs’. The company added that, along with its partner US generics maker Mylan, it ‘will work with the French and European regulatory authorities with regard to the follow-up inspection of the drug product facility and the Marketing Authorization Applications with the goal of an early reinspection’.
Biocon and Mylan are exclusive partners on a broad portfolio of biosimilars and insulin analogues [4].
Related article
Biocon and Mylan challenge Indian ban on trastuzumab ‘similar biologics’
References
1. GaBI Online - Generics and Biosimilars Initiative. Mylan and Biocon submit pegfilgrastim biosimilar to EMA [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Aug 11]. Available from: www.gabionline.net/Biosimilars/News/Mylan-and-Biocon-submit-pegfilgrastim-biosimilar-to-EMA
2. GaBI Online - Generics and Biosimilars Initiative. Mylan and Biocon submit trastuzumab biosimilar to EMA [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Aug 11]. Available from: www.gabionline.net/Biosimilars/News/Mylan-and-Biocon-submit-trastuzumab-biosimilar-to-EMA
3. GaBI Online - Generics and Biosimilars Initiative. Mylan and Biocon submit insulin glargine biosimilar to EMA [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Aug 11]. Available from: www.gabionline.net/Biosimilars/News/Mylan-and-Biocon-submit-insulin-glargine-biosimilar-to-EMA
4. GaBI Online - Generics and Biosimilars Initiative. Mylan and Biocon to parter on insulin products [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Aug 11]. Available from: www.gabionline.net/Biosimilars/News/Mylan-and-Biocon-to-partner-on-insulin-products
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: Biocon
Research
Positive safety and efficacy primary endpoint results for AVT05 (golimumab proposed biosimilar)
News
EMA recommends approval for tocilizumab biosimilar Avtozma and filgrastim biosimilar Zefylti
Ustekinumab biosimilars Yesintek, Steqeyma, and Otulfi approved by FDA, EMA and Health Canada
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
Biologicals and biosimilars available for IBD in Canada
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
SBR issues consensus on interchangeability of reference products and biosimilars
Innovative direct purchase agreement sees adalimumab biosimilar prices slashed
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia

Biosimilars/General Posted 20/11/2024
SBR issues consensus on interchangeability of reference products and biosimilars

Biosimilars/General Posted 13/11/2024
Innovative direct purchase agreement sees adalimumab biosimilar prices slashed

Biosimilars/General Posted 15/10/2024
The best selling biotechnology drugs of 2008: the next biosimilars targets

Post your comment