Lead Optimization and Preclinical Development of Human Nicotine-Specific mAbs

Information

  • Research Project
  • 8828430
  • ApplicationId
    8828430
  • Core Project Number
    R01DA038877
  • Full Project Number
    1R01DA038877-01
  • Serial Number
    038877
  • FOA Number
    PAR-13-334
  • Sub Project Id
  • Project Start Date
    9/30/2014 - 11 years ago
  • Project End Date
    7/31/2017 - 8 years ago
  • Program Officer Name
    KRIETER, PHILIP A
  • Budget Start Date
    9/30/2014 - 11 years ago
  • Budget End Date
    7/31/2015 - 10 years ago
  • Fiscal Year
    2014
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/15/2014 - 11 years ago

Lead Optimization and Preclinical Development of Human Nicotine-Specific mAbs

DESCRIPTION (provided by applicant): Cigarette smoking is responsible for >480,000 deaths per year in the United States. The CDC estimates direct healthcare costs due to treating smoking and smoking-related illness is >$133 billion/yr. Only 1:5 smokers achieve long-term abstinence using standard of care pharmacotherapies leaving the majority still smoking and seeking alternatives. We are developing nicotine-specific high-affinity human monoclonal antibodies (mAbs) as aids to smoking cessation treatment. Nicotine-specific mAbs (nic-mAbs) reduce nicotine distribution to the brain and demonstrate efficacy in animal models of nicotine dependence and withdrawal. The preclinical proof-of-concept has been well-documented with mouse nic-mAbs and human nic-mAb leads. Nic-mAbs can eliminate the high degree of inter-individual variability in immune response observed clinically for nicotine vaccines (quantity and quality). Nic-mAbs can provide the much needed control over inter-individual variability necessary to achieve clinical proof-of-concept of the PK mechanism of treating nicotine addiction. This Alliance is dedicated to developing nic-mAbs for clinical use. Several approaches are being undertaken to provide nic-mAb lead series for lead optimization and pre-clinical development. The programs are at various stages of development and encompass humanization of mouse nic-mAbs using routine genetic engineering techniques, selection from human b-cells that express high-affinity nic-mAbs from prior-vaccinated individuals, and screening a human phage display library for high-affinity Fab's. These parallel efforts, using different sources and methods, will improve our odds of success in selecting a development candidate with the desired characteristics to move ahead into IND-enabling studies. Each lead in a given nic-mAb series will be progressed through a variety of standardized in vitro assays and well-established in vivo studies in animal models of nicotine dependency and withdrawal. Our goal is to progress a development candidate to IND enabling studies in preparation for clinical investigational studies in man.

IC Name
NATIONAL INSTITUTE ON DRUG ABUSE
  • Activity
    R01
  • Administering IC
    DA
  • Application Type
    1
  • Direct Cost Amount
    2341858
  • Indirect Cost Amount
    211180
  • Total Cost
    2553038
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    279
  • Ed Inst. Type
  • Funding ICs
    NIDA:2553038\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZDA1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ANTIDOTE THERAPEUTICS, INC.
  • Organization Department
  • Organization DUNS
    079189618
  • Organization City
    BETHESDA
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    208173166
  • Organization District
    UNITED STATES