Biosimilar monoclonal antibody approved in Korea

Biosimilars/News | Posted 03/08/2012 post-comment0 Post your comment

South Korean biotechnology company Celltrion announced on 23 July 2012 that the Korean Food and Drug Administration (KFDA) had approved its first monoclonal antibody, Remsima.

picture 132

The drug is a biosimilar of Johnson & Johnson’s rheumatoid arthritis blockbuster Remicade (infliximab).

KFDA approval for Remsima is based on clinical trials carried out by Celltrion, the results of which were presented at the Annual Congress of the European League Against Rheumatism (EULAR) held in Berlin, Germany, on 6–9 June 2012 [1]. The trials demonstrated the similar pharmacokinetic profile, clinical efficacy and overall safety of Remsima (CT-P13) compared to Remicade.

Remsima was approved by KFDA for several indications, including treatment of rheumatoid arthritis, ankylosing spondylitis, ulcerative colitis, Crohn’s disease and psoriasis.

Celltrion is preparing to launch Remsima in approximately 100 countries including the EU and other developed markets. The company has already applied to EMA for approval of the biosimilar in the EU and intends to launch Remsima in Asia and South America by the end of 2012.

Celltrion, as a contract manufacturing organisation, has an agreement to develop and market eight biosimilars, including infliximab, with US-based generics major Hospira [2]. The company has at least six other biosimilars in various stages of development, covering indications such as breast cancer, Hodgkin’s lymphoma, colorectal cancer, colon cancer and respiratory syncytial virus. 

Related articles

Biosimilar infliximab equivalence proven in phase III trial

Phase I trial of biosimilar infliximab proves biosimilarity

References

1.  GaBI Online - Generics and Biosimilars Initiative. Trials of biosimilar monoclonal antibody prove biosimilarity [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2012 Aug 3]. Available from: www.gabionline.net/Biosimilars/News/Trials-of-biosimilar-monoclonal-antibody-prove-biosimilarity

2.  GaBI Online - Generics and Biosimilars Initiative. South Korea to emerge as global leader in biosimilar R & D [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2012 Aug 3]. Available from: www.gabionline.net/Biosimilars/News/South-Korea-to-emerge-as-global-leader-in-biosimilar-R-D

Source: Celltrion

comment icon Comments (0)
Post your comment
Related content
FDA approves filgrastim biosimilar Nypozi
Filgrastim Grastofil V13H23
Biosimilars/News Posted 04/09/2024
FDA approves third aflibercept biosimilar Ahzantive
Bevacizumab VEGF Lucentis V21D02MN
Biosimilars/News Posted 13/08/2024
China approves Simcare’s cetuximab beta Enlituo
Cancer Cell V13I20
Biosimilars/News Posted 30/07/2024
Most viewed articles
About GaBI
Home/About GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010