SBIR/STTR Research Award

Evaluation of High-Capacity Adenovectors in the Eye

Award identifier b7d4ca4e79a619bb3cc91086c765c74aa7a736a5830cacd048e5831e39df8f40Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$432,726

Program and phase

SBIR · Phase II

Award year

2005

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
GENVEC, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2005-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Exudative age-related macular degeneration (AMD) is due to aberrant neovascularization in the eye, and is one of the leading major causes of blindness in the U.S. Pigment Epithelium-Derived Factor (PEDF) is a potent angiogenic and neurotrophic factor and is a key regulator of vascularity in the eye. When delivered to the eye via an adenovirus vector, PEDF can block growth of new blood vessels and trigger the regression of established abnormal vessels in animal models for AMD and diabetic retinopathy. GenVec has recently demonstrated safety of an adenovector that expresses PEDF (AdPEDF. 11) in patients with AMD. However, two important risks to the commercialization of AdPEDF. 11 are transient PEDF expression that may require repeat administration and the potential for vector-induced inflammation at high doses, both of which have been observed in animal models. In this Phase II SBIR we propose to address these risks using high capacity (HC) adenovectors based on adenovirus type 5. This Small Business Innovation Research Phase II proposal aims take the next steps toward clinical testing of HC vectors. Building on successes in the Phase I effort the proposed research will provide breakthroughs needed to advance this promising vector system. The Specific Aims are: 1) To determine the full duration of increased PEDF expression in the eye following intravitreous delivery of HC.PEDF; 2) To test the hypothesis that long-term PEDF expression results in long-term ocular efficacy; 3) To build a system for the production of high quality HC vectors that is scalable, and applicable for GMP manufacturing. The results of these studies will provide critical elements of an IND submission. This SBIR proposal will allow direct application of HC technology to a rapidly advancing therapeutic product program. The long-term goal of this proposal is the clinical testing and commercialization of PEDF expressing HC vector for the treatment of AMD and other ocular neovascular diseases.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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