Increasing the efficacy of MTI-101 in MM using Ab conjugation strategies

Information

  • Research Project
  • 8591600
  • ApplicationId
    8591600
  • Core Project Number
    R43CA180308
  • Full Project Number
    1R43CA180308-01
  • Serial Number
    180308
  • FOA Number
    PA-12-088
  • Sub Project Id
  • Project Start Date
    7/31/2013 - 11 years ago
  • Project End Date
    1/30/2014 - 10 years ago
  • Program Officer Name
    HAIM, TODD E.
  • Budget Start Date
    7/31/2013 - 11 years ago
  • Budget End Date
    1/30/2014 - 10 years ago
  • Fiscal Year
    2013
  • Support Year
    01
  • Suffix
  • Award Notice Date
    7/31/2013 - 11 years ago

Increasing the efficacy of MTI-101 in MM using Ab conjugation strategies

DESCRIPTION (provided by applicant): The majority of multiple myeloma (MM) patients will initially respond to standard chemotherapy. However, eventually relapse of the disease, associated with a multi-drug resistant phenotype, contributes to poor clinical outcomes. Modulation Therapeutics is dedicated towards developing strategies for targeting cancers like MM that home or metastasize to the bone. Our current lead compound binds a CD44/VLA-4 complex and induces necrotic cell death. The in vivo efficacy of MTI-101 has been demonstrated using two in vivo myeloma models which consider the bone marrow microenvironment when evaluating tumor response. Our lead compound is a cyclic peptide which reduces concerns of proteolytic degradation. However, the efficacy of the compound may still be limited by a short circulating half-life often typical of peptide based therapies. The oveall goal of this proposal is to utilize antibody conjugation strategies designed to increase the therapeutic window of our lead compound. The first goal of this proposal is to determine whether conjugation of MTI-101 to a non-targeting antibody will increase the in vivo efficacy of the compound. The second goal of this proposal is to generate and evaluate a conjugate of MTI-101 and a CD138-targeting antibody to determine if we can increase specificity of the compound and thereby increase the therapeutic window of our lead compound.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    288301
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    395
  • Ed Inst. Type
  • Funding ICs
    NCI:288301\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    MODULATION THERAPEUTICS, INC.
  • Organization Department
  • Organization DUNS
    968675244
  • Organization City
    morgantown
  • Organization State
    WV
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    26506
  • Organization District
    UNITED STATES