Samsung Bioepis’ Flixabi® Infliximab Biosimilar Recommended for Approval in the European Union
INCHEON, Korea–(BUSINESS WIRE)– Samsung Bioepis Co., Ltd. today announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion on Flixabi ® – a biosimilar version of Remicade ® (infliximab), also known as SB2 – for the treatment of rheumatoid arthritis, Crohn’s disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis, and psoriasis. Flixabi ® is the second anti-TNF-α biosimilar developed by Samsung Bioepis to receive a positive recommendation for approval in Europe.
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This Smart News Release features multimedia. View the full release here: http://www.businesswire.com/news/home/20160401005635/en/ Christopher Hansung Ko, President & CEO of Samsung Bioepis (Photo: Business Wire)
The CHMP’s positive opinion will now be referred to the European Commission (EC) which will review and decide on the grant of a marketing authorization for Flixabi ®. If a marketing authorization is granted, Flixabi ® will be commercialized in the European Union (EU) by Biogen. “The CHMP’s positive opinion on Flixabi brings us a step closer to broadening affordable, high-quality treatment options for autoimmune patients across Europe,” said Christopher Hansung Ko, President & CEO of Samsung Bioepis. “We will continue to leverage our strengths in product development and quality assurance, so that we can increase patient access to a wider choice of life-enhancing medications.” The positive CHMP opinion on Flixabi ® was based on Phase 1 and Phase 3 clinical studies that tested the biosimilarity of Flixabi® to Remicade ®. In a 54-week Phase 3 clinical study, Flixabi ® showed comparable safety and equivalent efficacy to Remicade®, as evidenced in ACR20 response rate of 65.3% in the Flixabi ® arm versus 69.2% in the Remicade ® arm at Week 54, fully supporting the 30-week study results of 64.1% and 66.0%, respectively. The Flixabi ® study randomized 584 patients with moderate to severe rheumatoid arthritis despite methotrexate therapy across 73 sites in 11 countries. Samsung Bioepis Biosimilar Pipeline
Commercialization of Samsung Bioepis Biosimilars About Samsung Bioepis Co., Ltd. View source version on businesswire.com: http://www.businesswire.com/news/home/20160401005635/en/ Contacts Samsung Bioepis Co., Ltd. |