Coherus Awaits August 2022 Date As FDA Accepts Ranibizumab Biosimilar

Company Set For Showdown With Samsung Bioepis For Biosimilar Lucentis

The US FDA has accepted for review the CHS-201 Lucentis biosimilar product developed by Formycon/Bioeq that is to be sold in the US by Coherus BioSciences, shortly after approving the first ranibizumab biosimilar to treat wet age-related macular degeneration.

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Samsung Bioepis' Byooviz became the first FDA-approved Lucentis biosimilar last month • Source: Shutterstock

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