Topical Use of TEAC to Treat Cutaneous Viral Infection

Information

  • Research Project
  • 7111721
  • ApplicationId
    7111721
  • Core Project Number
    R44AI058358
  • Full Project Number
    5R44AI058358-03
  • Serial Number
    58358
  • FOA Number
  • Sub Project Id
  • Project Start Date
    7/1/2004 - 19 years ago
  • Project End Date
    1/31/2008 - 16 years ago
  • Program Officer Name
    BAKER, CARL
  • Budget Start Date
    8/1/2006 - 17 years ago
  • Budget End Date
    1/31/2008 - 16 years ago
  • Fiscal Year
    2006
  • Support Year
    3
  • Suffix
  • Award Notice Date
    8/1/2006 - 17 years ago

Topical Use of TEAC to Treat Cutaneous Viral Infection

[unreadable] DESCRIPTION (provided by applicant): Common warts, those found on the hands, tops of the feet, and sometimes on the face, arms and legs, may persist for years and may increase in size and number. Some warts may convert to cancers, and the wart virus, human papillomavirus, is the cause of cervical cancer accounting for more than 250,000 deaths annually of women worldwide. The objectives of this proposal are to develop marketable, topical formulations of tetraethylammonium chloride (TEAC) for the treatment of human papillomavirus-induced common warts. This work is directly related to the current support of FDA regulatory submissions for this indication. The proposal describes the manufacturing process, pharmacology, and toxicology studies (to establish safety and antiviral activity of the formulations), required to proceed forward with the series of FDA Phase l/ll clinical trials needed to establish therapeutic efficacy and safety in man. The initial formulation identification, optimization, and selection procedures (that include evaluation of the antiviral activity of promising formulations), were accomplished in the Phase I SBIR grant. This Phase II proposal includes: 1) Development of analytical methods for monitoring TEAC and its degradants; 2) Manufacture of formulations under Good Manufacturing Procedures for use in toxicology and clinical studies, as well as formulation stability studies; 3) Evaluation of the safety of TEAC formulations in animal models for primary skin and eye irritation; 4) Evaluation of TEAC formulation toxicity in a topical repeat-dose study in minipigs; 5) Clinical demonstration in a 21-day cumulative irritation study that the lead TEAC formulation is a non-irritant; and 6) Clinical demonstration of safety and efficacy of the lead TEAC formulation in a proof-of principle study in patients with common warts. TEAC, a compound with known antiviral activity, has a very promising safety profile in humans and affords a significant opportunity to become the first FDA-approved topical product for the treatment of common warts. [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R44
  • Administering IC
    AI
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    489383
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    856
  • Ed Inst. Type
  • Funding ICs
    NIAID:489383\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    DOW PHARMACEUTICAL SCIENCES
  • Organization Department
  • Organization DUNS
    194721510
  • Organization City
    PETALUMA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    94954
  • Organization District
    UNITED STATES