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Since launch in 2011, more than 2 million doses of eylea have been administered. The extension of review periods was due to a major amendment triggered by observations during an fda inspection, which may raise concerns about the. For additional safety information, please talk to your doctor and see the full prescribing information for eylea hd and eylea

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Despite the delay, eylea hd remains available in the u.s., and regeneron anticipates a swift resolution as they address manufacturing concerns and continue expanding treatment options. Potential negatives the fda has extended the target action dates for key regulatory submissions related to eylea hd, indicating potential delays in market launch and impacting the company's timeline for introducing new treatment options Find important resources for hcp’s to learn more about eylea® (aflibercept) injection for the treatment of wet amd, dme, dr, and mefrvo

See important safety info and review full prescribing information.

The company noted this would offer greater dosing flexibility for physicians and patients Eylea hd (aflibercept) injection 8 mg sbla accepted for fda priority review for both the treatment of macular edema following retinal vein occlusion (rov) and for monthly dosing in approved indications The fda accepts regeneron’s sbla for eylea hd under priority review, targeting rvo treatment and expanded monthly dosing options.