DEVELOPMENT OF A BIOPOLYMER-BASED TEAR FILM SUPPLEMENT

Information

  • Research Project
  • 6140450
  • ApplicationId
    6140450
  • Core Project Number
    R44EY012573
  • Full Project Number
    2R44EY012573-02
  • Serial Number
    12573
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/1/1999 - 25 years ago
  • Project End Date
    9/29/2002 - 22 years ago
  • Program Officer Name
    FISHER, RICHARD S
  • Budget Start Date
    9/30/2000 - 24 years ago
  • Budget End Date
    9/29/2001 - 23 years ago
  • Fiscal Year
    2000
  • Support Year
    2
  • Suffix
  • Award Notice Date
    9/18/2000 - 24 years ago

DEVELOPMENT OF A BIOPOLYMER-BASED TEAR FILM SUPPLEMENT

Current modeling of the tear film acknowledges a larger presence and role of mucin in its structure and function. The objective of this application is to produce a tear supplement of natural, purified mucin, and establish its effects on the structure, stability and lubrication of the tear film, using the clinical model accepted by the FDA. No available products have shown any treatment effect versus control (saline). This would therefore be a medical advance over all currently available products. The specific aims of Phase II of the proposed research are: 1. Validate the process for recovering milk mucin from acid dairy whey. 2. Continue characterization of the milk mucin from acid dairy whey, particularly with regard to any lipid complexing. 3. Perform the required preclinical testing and submit an investigational new drug (IND) application to the FDA. 4. Finalize the milk mucin based dry eye solution, guided by objective in- vivo tear film interferometry and clinical examination, as well as subjective grading of symptoms and comfort. 5. Assess the milk mucin based dry eye solution on eye to demonstrate proof of concept and establish clinical significance. 6. Prepare a business plan to present to potential partners and/or investors. PROPOSED COMMERCIAL APPLICATION: Our product would be an improvement over current commercial products in virtually all cases of dry eye. An FDA approved product that actually treats dry eye or relieves symptoms beyond that of placebo would increase the dollar value of the approximately $100 million dry eye market by opening up a non-OTC, therapeutic market that currently does not exist for dry eye.

IC Name
NATIONAL EYE INSTITUTE
  • Activity
    R44
  • Administering IC
    EY
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    427600
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    867
  • Ed Inst. Type
  • Funding ICs
    NEI:427600\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    VISTA SCIENTIFIC, LLC
  • Organization Department
  • Organization DUNS
  • Organization City
    ANDOVER
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    01810
  • Organization District
    UNITED STATES