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Treat with foresight
namd

nAMD

Unsurpassed and sustained vision gains with proactive extended dosing1,2

2X

Long-lasting VEGF-A suppression

Up to 2x  longer than ranibizumab3-5

proactive Extended dosing

Proactive extended dosing

By Week 96 in the ALTAIR study:

  • Up to 60% of patients reached an injection interval of ≥12 weeks1,2
  • Up to 46% of patients reached an injection interval of 16 weeks2
Decreased injection frequency

Decreased injection frequency

Achieve sustained VA gains with as few as 3 injections in Year 2 1

EYLEA®: YOUR CHOICE FOR FOR PROACTIVE TREAT AND EXTEND UP TO Q161

Sustained VEGF supression with EYLEA®1

Mean Duration

Mean duration of VEGF-A suppression with EYLEA®:67+/-14 days

Mean duration of VEGF-A suppression with ranibizumab 34+/-5days

 Definite VEGF suppression

 Uncertain suppression status

Uncertain end of suppression

 

Long-lasting anti-VEGF activity upto 2x longer than a ranibizumab (P<0.0001)4,5

VA GAINS MAINTAINED AT YEAR 2 WITH PROACTIVE EXTENDED DOSING2

Q12 and beyond: VA gains observed in Year 1 and Year 2 of ALTAIR1,2

Mean number of injections at 96 weeks for both groups: 10.4 injections2

ACHIEVE UNSURPASSED AND SUSTAINED VA GAINS WITH EYLEA®

Treat and extend patients up to Q161,2,6

    Proportion of patients
    Proportion of patients
    • Proportion of patients achieving ≥12-week dosing at 96 weeks
    • Proportion of patients achieving 16-week dosing at 96 weeks
    Proportion of patients
    Proportion of patients
    • Proportion of patients achieving ≥12-week dosing at 96 weeks
    • Proportion of patients achieving 16-week dosing at 96 weeks

    Achieve sustained VA gains with as few as 3 injections in Year 2 when proactive T&E is used with EYLEA®1,2

    Dosing
    MOA

    References:

    • EYLEA® (aflibercept solution for injection) Summary of Product Characteristics. Berlin, Germany: Bayer Pharma AG. Return to content
    • Ohji M, Takahashi K, Okada AA, Kobayashi M, Matsuda Y, Terano Y; for ALTAIR Investigators. Efficacy and safety of intravitreal aflibercept treat-and-extend regimens in exudative age-related macular degeneration: 52- and 96-week findings from ALTAIR: a randomized controlled trial [published online ahead of print February 3, 2020]. Adv Ther. doi: 10.1007/s12325-020-01236-x. Return to content
    • Muether PS, Hermann MM, Dröge K, Kirchhof B, Fauser S. Long-term stability of vascular endothelial growth factor suppression time under ranibizumab treatment in age-related macular degeneration. Am J Ophthalmol. 2013;156:989-993. Return to content
    • Fauser S, Muether PS. Clinical correlation to differences in ranibizumab and aflibercept vascular endothelial growth factor suppression times. Br J Ophthalmol. 2016;100:1494-1498. Return to content
    • Fauser S, Schwabecker V, Muether PS. Suppression of intraocular vascular endothelial growth factor during aflibercept treatment of age-related macular degeneration. Am J Ophthalmol. 2014;158:532-536. Return to content
    • Richard G, Monés J, Wolf S, et al. Scheduled versus pro re nata dosing in the VIEW trials. Ophthalmology. 2015;122:2497-2503. Return to content
    • Papadopoulos N, Martin J, Ruan Q, et al. Binding and neutralization of vascular endothelial growth factor (VEGF) and related ligands by VEGF Trap,ranibizumab and bevacizumab. Angiogenesis. 2012;15;171-185. Return to content