ABZYME THERAPEUTICS LLC — Department of Health and Human Services SBIR Phase I: N

Description

DESCRIPTION provided by applicant The age related macular degeneration AMD characterized by the formation of subretinal choroidal neovascularization is the main cause of blindness in the elderly Vascular endothelial growth factor VEGF regulates angiogenesis and enhances vascular permeability that results in visual acuity deterioration Blockade of VEGF action is currently the most effective strategy in preventing choroidal angiogenesis and reducing vascular permeability The intravitreal injection of anti VEGF drugs has been widely employed to reduce the disease progression and improve the visual outcomes of the affected patients Unfortunately intravitreal injection requires the administration in hospital poses a risk of sevee infection retinal detachment cataract endophthalmitis intraocular inflammation increase of intraocular pressure and vitreous hemorrhage as well as has low patient compliance Abzyme Therapeutics LLC proposes to develop a new therapeutic for self administrable noninvasive topical delivery to inhibit abnormal angiogenesis in the retina and choroid The anti neovascularization therapeutic for AMD treatment will be designed to overcome the retinal and choroidal barriers such that the therapeutic can be delivered in the form of eye drop Active anti angiogenesis therapeutics will reach the VEGF target in the vitreous humor via transferrin receptor TfR mediated transcytosis and transcorneal transport In Phase I human single domain high affinity anti VEGF neutralizing nanobodies and bispecific VEGF TfR nanobodies with low affinity to TfR and high affinity to VEGF will be produced The accumulation of nanobodies in the vitreous humor and retina will be determined in a mouse model that receives topical eye drops In Phase II the anti neovascularization activity of transferrin receptor mediated anti VEGF therapeutics will be characterized and validated in animal AMD models pursuing the IND application PUBLIC HEALTH RELEVANCE As a result of this project novel bispecific human nanobodies for treatment of age related macular degeneration will be produced The topical self administrable antibody based therapy in an outpatient setting will represent a major improvement in comparison with the current intravitreal injection by lowering the treatment cost while improving patient compliance and reducing potential side effects and complications