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Functional Characterization of Abicipar-Pegol, an Anti-VEGF DARPin Therapeutic That Potently Inhibits Angiogenesis and Vascular Permeability
Author(s) -
Gerard A. Rodrigues,
Matthew D. Mason,
LoriAnn Christie,
Candice Hansen,
Lisa M. Hernández,
James A. Burke,
Keith A. Luhrs,
Thomas C. Hohman
Publication year - 2018
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.18-25307
Subject(s) - vascular endothelial growth factor , angiogenesis , in vivo , neovascularization , pharmacology , vascular endothelial growth factor a , ranibizumab , vascular permeability , medicine , chemistry , cancer research , biology , bevacizumab , pathology , vegf receptors , microbiology and biotechnology , chemotherapy
DARPin molecules are a novel class of small proteins that contain engineered ankyrin repeat domain(s) and bind to target proteins with high specificity and affinity. Abicipar-pegol (abicipar), a DARPin molecule targeting vascular endothelial growth factor-A (VEGF-A), is currently under evaluation in patients with age-related macular degeneration. The pharmacodynamic properties of abicipar were characterized using in vivo and in vitro assays.

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