ONCOLYTIC HERPES SIMPLEX VIRUS TYPE 1 FOR TUMOR THERAPY

Information

  • Research Project
  • 2869176
  • ApplicationId
    2869176
  • Core Project Number
    R43CA081889
  • Full Project Number
    1R43CA081889-01
  • Serial Number
    81889
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/1/1999 - 25 years ago
  • Project End Date
    3/31/2000 - 24 years ago
  • Program Officer Name
    FORRY-SCHAUDIES, SUZANNE L.
  • Budget Start Date
    4/1/1999 - 25 years ago
  • Budget End Date
    3/31/2000 - 24 years ago
  • Fiscal Year
    1999
  • Support Year
    1
  • Suffix
  • Award Notice Date
    3/30/1999 - 25 years ago

ONCOLYTIC HERPES SIMPLEX VIRUS TYPE 1 FOR TUMOR THERAPY

Cancer is a principal cause of death in the United States and new approaches to prevent or treat the disease are clearly needed. Clinical studies using a tumor selective human adenovirus (ONYX-015) have demonstrated that a replication competent virus can be engineered to be safe, specific and in several cases cause tumor necrosis. These results have prompted evaluation of Herpes Simplex Virus type 1 (HSV-1) as an oncolytic virus. The overall goal of this research is to identify replication competent HSV-1 mutants capable of specifically replicating in cancer cells. Efforts will be focused (aim 1) on testing existing HSV-1 mutants deleted for accessory function(s) which could only be complemented by tumorigenic cells, (aim 2) on assessing the function of tumor suppressor gene p53 in the context of the viral infection (aim 3) on determining conditions for random mutagenesis of the HSV-1 genome. This will be used for phase II studies where unique mutants will be generated and selected based on preferential growth in cancer cells versus normal cells. PROPOSED COMMERCIAL APPLICATION: Replication competent oncolytic HSV-1 will be used to treat cancer. Productive infection by mutant/recombinant viruses will take place specifically in cancer cells causing lysis/necrosis of the tumor. The tumor therapy could be used through local or systemic delivery of the modified virus for specific or broad cancer types depending on the characteristic of the engineered viruses.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    395
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
  • Organization Name
    ONYX PHARMACEUTICALS
  • Organization Department
  • Organization DUNS
  • Organization City
    RICHMOND
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    94806
  • Organization District
    UNITED STATES