The European Medicines Agency’s (EMA’s) Committee for Medicinal Products for Human Use (CHMP) announced on 31 July 2013 that it had recommended granting of marketing authorization for a biosimilar follitropin alfa. While on 9 September 2013, the agency announced the approval of a new somatropin biosimilar.
EMA approves biosimilar follitropin alfa and somatropin
Biosimilars/News
|
Posted 20/09/2013
0
Post your comment
The follitropin alfa biosimilar (Ovaleap) is produced by generics giant Teva Pharmaceutical Industries. Ovaleap is a biosimilar of Merck’s in vitro fertilization drug Gonal-F, which contains recombinant follicle stimulating hormone (FSH), which helps egg development in the ovaries. There are currently no biosimilars of follitropin alfa available on the European market.
The somatropin biosimilar (Somatropin Biopartners) is manufactured by BioPartners, a Switzerland-based subsidiary of Polish biotech company Bioton. The drug is a biosimilar of Eli Lilly’s recombinant human growth hormone Humatrope, which is used for the treatment of growth failure in children.
Although there is already a somatropin biosimilar approved by EMA [1], Somatropin Biopartners is the first prolonged-release somatropin-containing medicinal product to receive a positive CHMP opinion.
The CHMP’s recommendation for Somatropin Biopartners will now be referred to the European Commission which grants approval for the European Union, Norway and Iceland. The Commision’s final approval is anticipated in the third quarter of 2013.
Related article
EMA approves first monoclonal antibody biosimilars
Reference
1. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Europe [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2013 Sep 20]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-Europe
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 © 2013 Pro Pharma Communications International. All Rights Reserved.
Source: EMA
Research
HHS push to ‘genericize’ biosimilars sparks backlash
Biosimilar interchangeability: a necessary fix, but not a silver bullet
General
Medicines for Europe calls for Biotech Act reforms to address ‘biosimilar void’
SBR issues position statement on safe originator biological/biosimilar interchangeability
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
Canada approves multiple denosumab and ustekinumab biosimilars as global competition grows
FDA approves Zimrixby (rituximab) and Garzulys (insulin aspart) biosimilars
EMA recommends approval for biosimilar pegfilgrastim Cavoley
FDA approves first interchangeable ranibizumab biosimilar Ranluspec
Canada approves multiple denosumab and ustekinumab biosimilars as global competition grows
Biosimilars/News Posted 15/09/2026
FDA approves Zimrixby (rituximab) and Garzulys (insulin aspart) biosimilars
Biosimilars/News Posted 02/09/2026
FDA approves first interchangeable ranibizumab biosimilar Ranluspec
Biosimilars/News Posted 04/08/2026
The best selling biotechnology drugs of 2008: the next biosimilars targets
Post your comment