About EYLEA Results of phase 3 trials are presented for EYLEA.1 See the data
EYLEA (aflibercept) Injection vial and packaging

Proven Results Across All Approved Indications

EYLEA indications are backed by 7 pivotal studies evaluating BCVA as measured by ETDRS* letters in over 3000 patients: VIEW 1 and VIEW 2 (Wet AMD) at 52 weeks, VISTA and VIVID (DME and DR in Patients with DME) at 52 and 100 weeks, GALILEO and COPERNICUS (MEfCRVO) at 24 weeks, and VIBRANT (MEfBRVO) at 24 weeks.1 When starting a patient on EYLEA, consider the body of evidence demonstrating proven results.1

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Accessing EYLEA Comprehensive support for you and your patients. Find support
Patient Support

We're committed to help ensure your eligible patients have access to EYLEA, regardless of insurance or coverage. 


Get help navigating the reimbursement process. Find enrollment forms, sample appeal letters, and more. 

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News Stay informed on current EYLEA clinical information, events, and more. Read the latest
06 June
REGENERON Announces an Increase in the Wholesale Acquisition Cost (WAC) Discount from 1.1% to 2.5% for Community-Based Physicians, Effective June 11
07 May
Update on Post-Marketing Reports of Intraocular Inflammation (IOI) Following Administration of EYLEA® (aflibercept) Injection
  • * Best Corrected Visual Acuity as measured by Early Treatment Diabetic Retinopathy Study
  • anti-VEGF = anti–Vascular Endothelial Growth Factor
  • AMD = Age-related Macular Degeneration
  • MEfRVO = Macular Edema following Retinal Vein Occlusion (includes Branch Retinal Vein Occlusion [BRVO] and Central Retinal Vein Occlusion [CRVO])
  • DME = Diabetic Macular Edema
  • DR = Diabetic Retinopathy
Important Safety Information and Indications
  • EYLEA® (aflibercept) Injection is contraindicated in patients with ocular or periocular infections, active intraocular inflammation, or known hypersensitivity to aflibercept or to any of the excipients in EYLEA.
Important Safety Information Important Prescribing Information

EYLEA® (aflibercept) Injection is indicated for the treatment of patients with

Please see the full Prescribing Information for EYLEA.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

The information provided in this site is intended only for healthcare professionals in the United States. The products discussed herein may have different product labeling in different countries.

  1. EYLEA® (aflibercept) Injection full U.S. Prescribing Information. Regeneron Pharmaceuticals, Inc. May 2017.