ANTIBODY TARGETING TO PSMA IN PROSTATIC TUMORS

Information

  • Research Project
  • 2776431
  • ApplicationId
    2776431
  • Core Project Number
    R43CA080398
  • Full Project Number
    1R43CA080398-01
  • Serial Number
    80398
  • FOA Number
  • Sub Project Id
  • Project Start Date
    2/18/1999 - 25 years ago
  • Project End Date
    3/30/2000 - 24 years ago
  • Program Officer Name
    SCHERBENSKE, M. JAMES
  • Budget Start Date
    2/18/1999 - 25 years ago
  • Budget End Date
    3/30/2000 - 24 years ago
  • Fiscal Year
    1999
  • Support Year
    1
  • Suffix
  • Award Notice Date
    2/18/1999 - 25 years ago

ANTIBODY TARGETING TO PSMA IN PROSTATIC TUMORS

Prostate-specific membrane antigen (PSMA) is an effective cell surface marker for prostatic epithelial cells and is increased in expression in prostatic cancer, particularly the more aggressive forms of the disease. We have prepared a panel of monoclonal antibodies for extracellular epitopes present on PSMA. Studies will be conducted to determine their potential suitability for in vivo targeting of therapeutics to prostatic tumors. Antigen binding affinity will be determined as will their intrinsic ability to elicit ADCC and CDC cell killing. Specificity of 125I-labeled antibody binding to PSMA expressing and non-expressing cells will be tested in vitro as well as biodistribution of labeled antibody in mice bearing tumors which are both expressors and non-expressors of PSMA. Based on these results, an initial test will be conducted to assess tumoricidal activity of a 90Y-labeled antibody in mice bearing PSMA expressing and non-expressing tumors. The results will provide definitive evidence to assess the potential of anti- PSMA antibody targeting of therapeutics in treatment of prostate cancer in humans. PROPOSED COMMERCIAL APPLICATIONS: There were 209,900 new cases of prostatic cancer diagnosed in 1997. Many of these patients have, or will develop, metastatic cancer which is resistant to presently available therapy. Application of antibody targeting of therapeutic agents to prostate cancer via markers such as prostate-specific membrane antigen should be specific and result in new means to treat advanced disease.

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
    ZRG2
  • Study Section Name
  • Organization Name
    NORTHWEST BIOTHERAPEUTICS, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    Bethesda
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    20814
  • Organization District
    UNITED STATES