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

Coherus BioSciences, Inc. has confirmed plans to launch Formycon/Bioeq’s Lucentis (ranibizumab) biosimilar in the US in the second half of 2022 after the US Food and Drug Administration accepted the filing for review, assigning a target action date of 2 August 2022.

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