Results 81 to 90 of about 8,597,475 (170)
Impact of Baseline Central Retinal Thickness on Outcomes in the VIVID-DME and VISTA-DME Studies
Purpose. To report the impact of baseline central retinal thickness (CRT) on outcomes in patients with diabetic macular edema (DME) in VIVID-DME and VISTA-DME. Methods.
Edoardo Midena +5 more
doaj +1 more source
Purpose : In PULSAR (NCT04423718), the primary endpoint of change from baseline in best-corrected visual acuity at Week 48 (non-inferiority margin at 4 letters) was met with intravitreal aflibercept 8 mg every 12 or 16 weeks (8q12 or 8q16) vs aflibercept
SCHMIDT-OTT, Ursula Maria +4 more
core +1 more source
International audiencePurpose : To evaluate aflibercept 8 mg vs aflibercept 2 mg in patients with treatment-naïve neovascular age-related macular degeneration (nAMD). Methods : PULSAR (NCT04423718) is a double-masked, 96-week, Phase 3 trial.
Sivaprasad, S. +1 more
core
PURPOSE: To evaluate the 1-year efficacy and safety of aflibercept 8 mg compared with aflibercept 2 mg in a pre-specified analysis of patients from Japan with neovascular age-related macular degeneration (nAMD) included in PULSAR.
Zhang, Xin +18 more
core +1 more source
Background Aflibercept 8 mg was developed to extend treatment intervals in neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME). Although pivotal trials reported low rates of intraocular inflammation (IOI), post-marketing
Christos Papadimitriou +4 more
core +1 more source
Noninfectious Intraocular Inflammation After Intravitreal Aflibercept.
IMPORTANCE: Aflibercept, 8 mg, is an anti-vascular endothelial growth factor (VEGF) formulation for neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME).
Binder, Karoline E;Bleidißel, Nathalie;Charbel Issa, Peter;Maier, Mathias;Coulibaly, Leonard M
core +1 more source
To compare the efficacy and safety of the proposed aflibercept biosimilar SCD411 and reference aflibercept in patients with neovascular age-related macular degeneration, this randomized, double-masked, parallel-group, multicenter study was conducted in ...
Se Woong Kang +8 more
doaj +1 more source
Purpose: To report an unusual case of a patient with intractable central serous chorioretinopathy with a dramatic treatment response to high-dose intravitreal aflibercept. Methods: Retrospective case report.
Jonathan B. Lin, Loh-Shan B. Leung
doaj +1 more source
Objective Biosimilars are helping to reduce the cost burden of treatment and widen patient access to therapies. This multicentre trial compared the efficacy, safety and immunogenicity of the biosimilar aflibercept FYB203 with reference aflibercept in ...
András Papp +6 more
doaj +1 more source
Stephane A Régnier,1 William Malcolm,2 Jennifer Haig,3 Weiguang Xue41Novartis Pharma AG, Basel, Switzerland; 2Novartis Pharmaceuticals UK Ltd, Frimley Business Park, UK; 3Optum, Burlington, ON, Canada; 4Optum, Uxbridge, UKBackground: Ranibizumab ...
Xue W +3 more
core

