FDA Approves Extended Dosing Interval for Regeneron’s EYLEA HD (aflibercept)
FDA Approves Extended Dosing Interval for Regeneron’s EYLEA HD (aflibercept)
On April 2, 2026, Regeneron Pharmaceuticals announced that the U.S. Food and Drug Administration has approved an extension to the dosing intervals for EYLEA HD (aflibercept) patients with wet age-related macular degeneration (wAMD) and diabetic macular edema (DME). ... By: Goodwin