Bayer Ag · XETR:BAYN
Bayer — 23rd European Society of Retina Specialists (EURETINA) Congress 2023
10 slides from Bayer's conference presentation, October 2023
Slide 1: Subgroup Analyses from the Phase 3 PULSAR Trial of Aflibercept 8 mg in nAMD
Subgroup Analyses from the Phase 3 PULSAR Trial of Aflibercept 8 mg in Patients with Treatment-Naïve Neovascular Age-Related Macular Degeneration Oliver Zeitz,1 Sobha Sivaprasad,2 Sergio Leal,3 Tobias Machewitz,4 Xin Zhang,3 on behalf of the PULSAR study investigators 1Department of Ophthalmology, C
Slide 2: Disclosures
Disclosures nAMD • OZ: Consultant and speaker for Allergan, Bayer, Boehringer Ingelheim, and Novartis; is a consultant for Omeicos and Oxular; and receives research support from Bayer, Boehringer Ingelheim, and Novartis. Employment with Bayer ended September 30, 2016 o SS: receives funding/fees from
Slide 3: PULSAR Study Design
PULSAR Study Design Multicenter, randomized, double-masked study in patients with treatment-naive nAMD Randomized at baseline 1 (2q8) : 1 (8q12) : 1 (8q16) 2q8 Aflibercept 2 mg every 8 weeks after 3 initial monthly injections n=336 Primary endpoint at Week 48 Mean change in BCVA (non-inferiority) Ke
Slide 4: PULSAR: Dosing Schedule and Regimen Modification in Year 1
PULSAR: Dosing Schedule and Regimen Modification in Year 1 nAMD
Slide 5: BCVA by Baseline BCVA Categories (ETDRS Letters): At Week 48
BCVA by Baseline BCVA Categories (ETDRS Letters): At Week 48 nAMD
Slide 6: BCVA by Baseline CST Categories (µm): At Week 48
BCVA by Baseline CST Categories (µm): At Week 48 nAMD
Slide 7: BCVA by Baseline CNV Type: At Week 48
BCVA by Baseline CNV Type: At Week 48 nAMD
Slide 8: BCVA by Race: At Week 48
BCVA by Race: At Week 48 nAMD Change from Baseline at Week 48a
Slide 9: Proportion of Patients Maintaining 8 mg Q12 and Q16 Treatment Intervals Up to Week 48
Proportion of Patients Maintaining 8 mg Q12 and Q16 Treatment Intervals Up to Week 48: nAMD Categorized by Race
Slide 10: Conclusions: Baseline Subgroup Analyses at Week 48 nAMD
Conclusions: Baseline Subgroup Analyses at Week 48 nAMD • BCVA outcomes were comparable for aflibercept 8 mg vs aflibercept 2 mg among the evaluable subgroups of baseline characteristics • Regardless of differences in baseline BCVA and BCVA change at Week 48 in some subgroups, absolute BCVA values a
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