The Power Demonstrated With EYLEA—Proven Results Across All Approved Indications1

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 and 96 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

EYLEA (aflibercept) Injection 2 mg/0.05 mL single-use vial and packaging

Empower your EYLEA treatment decisions from the start with RESULTS from the 7 pivotal trials1

  • *Best-corrected visual acuity
  • Early Treatment Diabetic Retinopathy Study
  • anti-VEGF = anti–vascular endothelial growth factor
  • AMD = Age-related Macular Degeneration
  • DME = Diabetic Macular Edema
  • DR = Diabetic Retinopathy
  • RVO = Retinal Vein Occlusion (includes Branch Retinal Vein Occlusion [BRVO] and Central Retinal Vein Occlusion [CRVO])
EYLEA4U® logo
EYLEA (aflibercept) Injection co-pay card

No Matter What the Approved Indication, EYLEA Has More Than 90% First-Line Coverage Nationally*,2

First-line coverage means direct access to EYLEA—access that supports your treatment choice from the start.2 And, if patients need help paying for treatment, EYLEA4U® can assist in finding support options to help them with the cost.

*Individual patient coverage is subject to a patient's specific plan.

In My Eyes by Regeneron logo

Experience what certain retinal diseases can be like in virtual reality

Retinal disease virtual and augmented reality app

A powerful teaching tool to use with your patients and caregivers, this unique app lets the user experience retinal disease symptoms firsthand in a 360° view. In My Eyes uses virtual reality and augmented reality to show the impact of vision impairment on everyday situations.

  • Available on the App Store
  • Android app on Google play
Retinal disease virtual and augmented reality app
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 INDICATIONS

EYLEA® (aflibercept) Injection is indicated for the treatment of patients with Neovascular (Wet) Age-related Macular Degeneration (AMD), Macular Edema following Retinal Vein Occlusion (RVO), Diabetic Macular Edema (DME), and Diabetic Retinopathy (DR) in patients with DME.

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.

References
  1. EYLEA® (aflibercept) Injection full U.S. Prescribing Information. Regeneron Pharmaceuticals, Inc. August 2018.
  2. Data on file. Regeneron Pharmaceuticals, Inc. Zitter Health Insights Policy Access & Tracking Tool for Ophthalmology Trends in the Marketplace. Quarter 1: 2018.