Targeting Telomerase to Treat Ocular Neovascular DisordersTherapeutic strategies for treating ocular neovascular disorders by targeting telomerase. Choroidal neovascularization (CNV) is the principal driver of blindness in neovascular age-related macular degeneration (nvAMD). Abnormal blood vessel growth beneath the macular leads to retinal damage and severe vision loss. Discovering the involvement of VEGF in the underlying mechanisms driving ocular angiogenesis has resulted in the development of multiple VEGF-targeted ocular therapeutics where none had previously existed.
The Need Current therapies for ocular neovascular disorders targeting VEGF, while effective, pose challenges such as adverse effects on retinal cells and decreased efficacy over time. There is a critical need for alternative treatments that target neovascularization with minimal impact on normal ocular function and provide sustained efficacy.
The Technology Researchers at The Ohio State University have developed a novel therapeutic for ocular disorders involving neovascularization that focuses on targeting telomerase to inhibit the development of choroidal neovascularization (CNV). Through genetic and pharmacological approaches, the novel technology suppresses telomerase activity, effectively reducing CNV growth. This non-viral therapeutic strategy offers a promising alternative to conventional anti-VEGF therapies, potentially mitigating their adverse effects while maintaining therapeutic efficacy. Commercial Application
Benefits/Advantages
Patent application pending |
Tech IDT2024-076 CollegeLicensing ManagerWillson, Christopher InventorsCategories |