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Samsung Bioepis Scoops First EU Lucentis Biosimilar As 2022 Date Looms

Byooviz Biosimilar Backed By EMA Committee In June

 
• By Dean Rudge

Samsung Bioepis has seen a positive opinion in the EU for its Byooviz (ranibizumab) biosimilar treatment for wet age-related macular degeneration turned into final approval by the European Commission. The company is also leading the pack in the US.

Eye
Byooviz is to be marketed in Europe by Biogen • Source: Shutterstock

Samsung Bioepis Co., Ltd. is poised to be among the first wave of biosimilars to Lucentis (ranibizumab) in Europe, after the European Commission granted final approval for the Korean firm’s marketing authorization application.

Approval had been keenly anticipated, following a positive opinion adopted by the European Medicines Agency’s Committee for Medicinal Products for Human Use in June for the company’s Byooviz

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