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FDA accepts sBLA for 16 week dosing regimen of Eylea® (aflibercept)

Jun 29, 2022

Regeneron announced that the FDA has accepted for review the sBLA for Eylea® (aflibercept) for a 16-week 2mg dosing regimen (after initial monthly doses) in patients with diabetic retinopathy.  The FDA has set a target action date of 28 February 2023.