Amgen Confirms US Aflibercept Filing As Regeneron Awaits Biocon Trial Fate

Key Exclusivity In May 2024, But Feeling Is That H2 2025 Launch More Likely

Amgen has thrown its hat in the ring to launch a US biosimilar to Regeneron’s Eylea eye-disease blockbuster, as all eyes remain on the outcome of a key patent-infringement trial between Biocon and the originator.

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As the clock ticks closer potentially on one of the largest biologic opportunities in the US in the current decade, Amgen has confirmed that the US Food and Drug Administration has accepted for filing its ABP 938 proposed biosimilar to Eylea (aflibercept) 2mg.

The California-based biotech had earlier unveiled positive results from its Phase III comparison trial for ABP 938 in patients with...

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An abbreviated licensure pathway for biologics was created by the 2009 Biologics Price Competition and Innovation Act. Biologics demonstrated to be biosimilar to or interchangeable with FDA-approved products can use the 351(k) biologics license application pathway. Biosimilars BLAs submitted under the 351(k) pathway have a 12 month user fee goal for FDA action. Updated weekly.

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