mCNV
mCNV

Strong, rapid, and sustained visual gains over 48 weeks

MOST VISUAL GAINS WERE ACHIEVED WITH 1 OR 2 INJECTIONS

EYLEA® 2mg-treated patients had a mean gain of +12.1 letters and 39% gained ≥3 lines at Week 24,increasing to +13.5 letters and 50% with ≥3 lines gained at Week 48

WEEK 48

WEEK 48
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Mean change in BCVA through Week 100

Mean change in BCVA through Week 100
  • Blue Circle
    EYLEA® 2mg administered at baseline and monthly up to Week 44 if mCNV persisted or recurred; n=90.
  • Blue Circle
    Sham injection administered at baseline up to Week 20 regardless of whether re-treatment criteria were fulfilled or not, followed by EYLEA® 2mg at Week 24 and monthly if disease persisted/recurred up to Week 44; n=31.
  • mCNV lesion size was reduced by >50% from baseline to Week 24 in the early EYLEA® 2mg treatment group.
  • Lesion size almost doubled in the delayed treatment group.
  • mCNV leakage was resolved by Week 48 in 86% of early EYLEA® 2mg-treated patients vs. 67% in the delayed treatment group.

DOSING

Pro-active dosing options across indications

DOSING

MOA

Unique multi-targeted trap mechanism

MOA

BCVA, best-corrected visual acuity; mCNV, myopic choroidal neovascularization; CRT, central retinal thickness; ETDRS, Early Treatment Diabetic Retinopathy Study; RCT, randomized controlled trial; VA, visual acuity.

PP-EYL-IL-0128-1


    • 1
      Ikuno Y, Ohno-Matsui K, Wong TY
      et al
      . Intravitreal aflibercept injection in patients with myopic choroidal neovascularization: The MYRROR study. Ophthalmology. 2015;122(6):1220–1227.
    • 2
      EYLEA® 2mg updated SPC as approved by the Israeli MoH.