Generation of a Novel Therapeutic for Prostate Cancer Bone Metastasis

Information

  • Research Project
  • 7803094
  • ApplicationId
    7803094
  • Core Project Number
    R43CA139965
  • Full Project Number
    1R43CA139965-01A1
  • Serial Number
    139965
  • FOA Number
    PA-09-080
  • Sub Project Id
  • Project Start Date
    9/1/2010 - 14 years ago
  • Project End Date
    5/31/2013 - 11 years ago
  • Program Officer Name
    LOU, XING-JIAN
  • Budget Start Date
    9/1/2010 - 14 years ago
  • Budget End Date
    5/31/2013 - 11 years ago
  • Fiscal Year
    2010
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    8/31/2010 - 14 years ago
Organizations

Generation of a Novel Therapeutic for Prostate Cancer Bone Metastasis

DESCRIPTION (provided by applicant): Prostate cancer is the third most common form of cancer in the US with an estimated 186,320 new cases in 2008 and 28,660 associated deaths. There are no curative treatments for metastatic prostate cancer. The annual cost of treating prostate cancer in the US is approximately 8 billion dollars. The end points of this proposal are to generate a new drug candidate, CT400P, and demonstrate therapeutic activity in a model of prostate cancer bone metastasis. CT400 is an engineered form of FGF1 that is designed to broadly antagonize functions of FGFs including angiogenesis, tumor growth and tumor resistance to chemotherapy. CT400 has previously demonstrated efficacy in a model of breast cancer. A PEGylated form of CT400 (CT400P) will be generated to increase solubility, circulatory half-life and potentially decrease immunogenicity. The PEGylated form of CT400 will be selected based on possessing key CT400 activities and enhanced drug-like properties. Thus CT400P must maintain: 1) high affinity for FGFRs and lack of integrin binding, 2) efficient antagonism of FGF1 and FGF2- induced cell proliferation, and 3) efficient reversal of cancer cell chemoresistance. CT400P will then be tested for efficacy in a mouse model of prostate cancer bone metastasis. The pharmacokinetic profile and/or tissue half-life will be determined to develop a dosing schedule. CT400P will be administered therapeutically, subsequent to establishing tumor growth. The efficacy of CT400P will be determined primarily by measuring changes in tumor growth. Having demonstrated proof of concept in a prostate cancer model CT400P will progress toward becoming a new therapeutic to treat prostate cancer and ultimately other types of cancers. PUBLIC HEALTH RELEVANCE: The goal of this proposal is to generate a new drug candidate and demonstrate therapeutic activity in a model of prostate cancer. It is anticipated that this therapeutic will be developed to treat prostate cancer for which there are 190,000 new cases with 29,000 associated deaths annually in the US. This new drug may ultimately be used to treat several types of cancer.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    233530
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    395
  • Ed Inst. Type
  • Funding ICs
    NCI:233530\
  • Funding Mechanism
    SBIR-STTR
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    CISTHERA, INC.
  • Organization Department
  • Organization DUNS
    808027994
  • Organization City
    SEATTLE
  • Organization State
    WA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    981038602
  • Organization District
    UNITED STATES