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Bispecific VEGF-A and Angiopoietin-2 Antagonist RO-101 Preclinical Efficacy in Model of Neovascular Eye Disease.
- Source :
-
Ophthalmology science [Ophthalmol Sci] 2024 Jan 18; Vol. 4 (4), pp. 100467. Date of Electronic Publication: 2024 Jan 18 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- Objective: To investigate preclinical data regarding the efficacy and biocompatibility of a bispecific protein, RO-101, with effects on VEGF-A and angiopoietin-2 (Ang-2) for use in retinal diseases.<br />Design: Experimental study.<br />Subjects: Brown Norway rats and New Zealand White Cross rabbits.<br />Methods: Preclinical study data of RO-101 in terms of target-specific enzyme-linked immunosorbent assay binding affinity to VEGF-A and Ang-2, vitreous half-life, inhibition of target-receptor interaction, laser choroidal neovascular membrane animal model, human umbilical vein endothelial cell migration, and biocompatibility was obtained. Where applicable, study data were compared with other anti-VEGF agents.<br />Main Outcome Measures: Binding affinity, half-life, biocompatibility, and efficacy of RO-101. Neovascularization prevention by RO-101.<br />Results: RO-101 demonstrated a strong binding affinity for VEGF-A and Ang-2 and in vitro was able to inhibit binding to the receptor with higher affinity than faricimab. The half-life of RO-101 is comparable to or longer than current VEGF inhibitors used in retinal disease. RO-101 was found to be biocompatible with retinal tissue in Brown Norway rats. RO-101 was as effective or more effective than current anti-VEGF therapeutics in causing regression of neovascular growth in vivo.<br />Conclusions: RO-101 is a promising candidate for use in retinal diseases. In preclinical models, RO-101 demonstrated similar or higher regression of neovascular growth to current anti-VEGF therapeutics with comparable or longer half-life. It also demonstrates a strong binding affinity for VEGF-A and Ang-2. It also was shown to be biocompatible with retinal tissue in animal studies, indicating potential compatibility for use in humans.<br />Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.<br /> (© 2024 by the American Academy of Ophthalmology.)
Details
- Language :
- English
- ISSN :
- 2666-9145
- Volume :
- 4
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Ophthalmology science
- Publication Type :
- Academic Journal
- Accession number :
- 38591047
- Full Text :
- https://doi.org/10.1016/j.xops.2024.100467