Evaluation of High-Capacity Adenovectors in the Eye

Information

  • Research Project
  • 6992781
  • ApplicationId
    6992781
  • Core Project Number
    R44EY015027
  • Full Project Number
    2R44EY015027-02
  • Serial Number
    15027
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/2003 - 21 years ago
  • Project End Date
    8/31/2007 - 17 years ago
  • Program Officer Name
    WUJEK, JEROME R
  • Budget Start Date
    9/30/2005 - 19 years ago
  • Budget End Date
    8/31/2006 - 18 years ago
  • Fiscal Year
    2005
  • Support Year
    2
  • Suffix
  • Award Notice Date
    9/19/2005 - 19 years ago
Organizations

Evaluation of High-Capacity Adenovectors in the Eye

[unreadable] 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. [unreadable] 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. [unreadable] 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. [unreadable] [unreadable]

IC Name
NATIONAL EYE INSTITUTE
  • Activity
    R44
  • Administering IC
    EY
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    215409
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    867
  • Ed Inst. Type
  • Funding ICs
    NEI:215409\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    GENVEC, INC.
  • Organization Department
  • Organization DUNS
    806729547
  • Organization City
    GAITHERSBURG
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    208784021
  • Organization District
    UNITED STATES