You are here

ShH10-Mediated Long-Term Delivery of Neurotrophic Factors in Animal Models of Gla

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41EY022848-01
Agency Tracking Number: R41EY022848
Amount: $1,387.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NEI
Solicitation Number: PA11-097
Timeline
Solicitation Year: 2012
Award Year: 2012
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
2749 CAROLINA AVE
REDWOOD CITY, CA 94061-3244
United States
DUNS: 16412260
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 ANNA DEMETRIADES
 (650) 924-1324
 and9059@med.cornell.edu
Business Contact
 THOMAS CHALBERG
Phone: (650) 924-1324
Email: tom@avalanchebiotech.com
Research Institution
 CORNELL UNIVERSITY
 
CORNELL UNIVERSITY ITHACA, NY 14853
ITHACA, NY 14853-
United States

 () -
 Nonprofit College or University
Abstract

DESCRIPTION (provided by applicant): The objective of this proposal is to examine the efficacy of a novel adeno-associated virus (AAV) variant, ShH10, expressing neurotrophic factors for the treatment of glaucoma. Glaucoma is the second leading cause of blindness with high associated societal costs, and is expected to grow. The hallmark of glaucoma is retinal ganglion cell (RGC) death, which leads to optic nerve degeneration and vision loss. Current treatment strategies are limited to pharmacotherapy and surgery to lower intraocular pressure; many patients progress, however, despite adequately controlled pressure. Therefore new treatment strategies are needed for glaucoma, including those that target RGC survival. Although neurotrophic factors, including BDNF, NT4, and GDNF, have shown promise for glaucoma, they are rapidly cleared from the eye, and frequent intraocular injections are not practical for this chronic, slow- progressing disease. Recently, a variant of adeno-associated virus, called ShH10, has shown promise for the long-term delivery of neurotrophic factors to the retina. In this Phase I proposal, we plan to characterize the value of ShH10 for delivery of neurotrophic factors in two animal models of glaucoma, and identify the most promising neurotrophic factor for future development. If this Phase I project demonstrates efficacy of ShH10- mediated neurotrophic factor delivery, these experiments will lay the groundwork for Phase II studies to further substantiate the promise of this approach, including large-animal efficacy and toxicology studies, as a treatment for glaucoma. PUBLIC HEALTH RELEVANCE: Glaucoma is the second leading cause of blindness worldwide, affecting over 2.2 million Americans and costing over 1.5 billion annually. Current strategies are limited to pressure-lowering eyedrops and surgeries, but despite adequately controlled pressure, many patients suffer poor outcomes. We propose to develop a new therapy that targets the survival of retinal neurons to improve the health outcomes for patients suffering from glaucoma.

* Information listed above is at the time of submission. *

US Flag An Official Website of the United States Government