MODIFIED TNF-ALPHA: AN ANTI CANCER THERAPY

Information

  • Research Project
  • 6338034
  • ApplicationId
    6338034
  • Core Project Number
    R43CA085023
  • Full Project Number
    1R43CA085023-01A2
  • Serial Number
    85023
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/4/2001 - 23 years ago
  • Project End Date
    2/3/2002 - 23 years ago
  • Program Officer Name
    MUSZYNSKI, KAREN
  • Budget Start Date
    4/4/2001 - 23 years ago
  • Budget End Date
    2/3/2002 - 23 years ago
  • Fiscal Year
    2001
  • Support Year
    1
  • Suffix
    A2
  • Award Notice Date
    4/4/2001 - 23 years ago

MODIFIED TNF-ALPHA: AN ANTI CANCER THERAPY

DESCRIPTION (PROVIDED BY APPLICANT): The long-term goal of the proposed research is the development of effective anti-cancer agents, modified human tumor necrosis factor-alphas (hTNFas). TNFa is a potent anti-neoplastic agent but its therapeutic application has been limited by its significant side effects. However, TNFa can be modified so that it retains its anti-tumor activities while its deleterious effects are reduced. This has been accomplished by mutation of TNFa and derivitization of TNFa with polyethylene glycol (PEG). This proposal focuses on the characterization and comparison of mutant and wild hTNFas modified with 20 kDa PEGs. The specific aims are to: 1) pharmacologically characterize the PEG-hTNFas, toxicity analyses after a single high dose of PEG-TNFa and a prolonged PEG-TNFa treatment; 2) define TNFa anti-cancer features, analyses of: a)anti-tumor efficacies in syngeneic and athymic mice with B16 melanomas, b)affinities of the PEG- hTNFas for hTNF receptors I and II (prerequisite for clinical trials); and 3) determine the anti-human tumor efficacies of these PEG-hTNFas, treatment of athymic mice bearing human colon carcinomas. PROPOSED COMMERCIAL APPLICATION: This proposal focuses on the development of new therapeutic agents, PEG-hNTFas effective against a wide range of solid tumors. Novel geatures of modified hTNFas include the likelihood of a marked synergy with cytotoxic chemotherapeutic agents and the potential to target the tumor vasculature and the host immune system.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    99962
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    395
  • Ed Inst. Type
  • Funding ICs
    NCI:99962\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    PHOENIX PHARMACOLOGICS, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    LEXINGTON
  • Organization State
    KY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    40506
  • Organization District
    UNITED STATES