Lateral Flow Immunoassay for Therapeutic Monoclonal Antibody Quality Assurance

Information

  • Research Project
  • 8648070
  • ApplicationId
    8648070
  • Core Project Number
    R43CA183241
  • Full Project Number
    1R43CA183241-01
  • Serial Number
    183241
  • FOA Number
    PA-13-088
  • Sub Project Id
  • Project Start Date
    4/15/2014 - 10 years ago
  • Project End Date
    4/14/2015 - 9 years ago
  • Program Officer Name
    RAHBAR, AMIR M.
  • Budget Start Date
    4/15/2014 - 10 years ago
  • Budget End Date
    4/14/2015 - 9 years ago
  • Fiscal Year
    2014
  • Support Year
    01
  • Suffix
  • Award Notice Date
    4/16/2014 - 10 years ago
Organizations

Lateral Flow Immunoassay for Therapeutic Monoclonal Antibody Quality Assurance

DESCRIPTION (provided by applicant): Monoclonal antibodies (mAb) are valuable therapeutics for treating cancer and other diseases, but their high cost makes them attractive targets for counterfeiting or illegal distribution. Numerous cases have occurred both in the US and worldwide and the complexity of the pharmaceutical distribution network makes the problem likely to persist. The goal of this project is to develop a simple and inexpensive lateral flow immunoassay that can be used to quickly determine the integrity of a monoclonal antibody therapeutic. Using mimetope peptides that mimic the native antigen epitope recognized by a give mAb, our test will discriminate between active mAb and other protein or immunoglobulin contaminants. Mimetope peptides have been developed for the top three mAb used in oncology: bevacizumab, trastuzumab, and rituximab. The rituximab mimetopes have already been developed in an ELISA format and used for pharmacokinetic studies, the remaining two will be similarly validated in Aim 1 of this proposal. In Aim 2, we will translate the ELISA assay to the lateral flow immunoassay format. In Aim 3 we will collaborate with a top clinician-scientist at the Moores UCSD Cancer Center to conduct a double blind study of the prototype tests for each of the mAb, determining their accuracy as well as their ability to detect either saline or polyclonal human immunoglobulin. Successful development of these products will enable oncologists and their patients to have added confidence that these potentially life-saving therapies are genuine and active at the time of administration.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    172406
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    395
  • Ed Inst. Type
  • Funding ICs
    NCI:172406\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ABREOS BIOSCIENCES, INC.
  • Organization Department
  • Organization DUNS
    068800915
  • Organization City
    SAN DIEGO
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    921224126
  • Organization District
    UNITED STATES