SBIR/STTR Research Award

Novel BIV-based vectors with retina-specific promoter

Award identifier 2516484893f43f1e97b6d689a993af1d3660546c5d2b7da4f35da7a66b102477Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$107,000

Program and phase

SBIR · Phase I

Award year

2005

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Cytopro, 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): Choroidal NeoVascularization (CNV) occurring in wet age-related macular degeneration (AMD) and diabetic proliferative retinopathy (DPR) is a chronic process leading to severe visual loss and blindness. CNV is characterized by growth of abnormal, new blood vessels from the choriocapillaris through defects in the Bruch's membrane into the sub-retinal space. The products currently in development are significantly compromised by the requirement for repeated and inconvenient intraocular injection. Thus, a better delivery system is needed. The strategy of treating CNV with anti-angiogenic factors is very promising. CytoPro aims the strategy that a single intra-ocular administration of a gene transfer vector will provide sustained delivery of a therapeutic, antiangiogenic protein selectively to the retina. CytoPro is now developing an advanced gene transfer system for potent anti-angiogenic transgenes to rapidly develop a superior product and to market it for CNV treatments. The goal of Phase I study of this SBIR project in the next few months is to develop a Cyto-PO promoter derived from human Pax6 PO promoter for gene delivery and expression using a lentiviral transfer system. In phase I of the project, we plan to: 1) optimize the efficiency and retina-specificity of the Cyto-PO promoter; 2) replace the viral origin CMV promoter in the lentiviral transfer vector; and 3) evaluate the specificity, efficiency and stability of the new lenti-Cyto-PO vector-mediated gene expression in retina-serived cells. We believe that objectives of phase I studies will be to accrue sufficient data for phase II studies that lenti-Cyto-PO vector system will be used in the retina of mice as a vehicle to transfer transgenes encoding anti-angiogenic peptides and siRNA to protect hypoxia-induced CNV. This tissue-specific lentiviral transfer system has tremendous commercial values because it will be very effective for the use of treating CNV in degenerative ocular diseases.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.