ST-246 treatment of smallpox vaccine-related adverse events

Information

  • Research Project
  • 7747102
  • ApplicationId
    7747102
  • Core Project Number
    R44AI075747
  • Full Project Number
    2R44AI075747-03
  • Serial Number
    75747
  • FOA Number
    PA-06-134
  • Sub Project Id
  • Project Start Date
    8/1/2007 - 17 years ago
  • Project End Date
    8/31/2012 - 12 years ago
  • Program Officer Name
    CHALLBERG, MARK D.
  • Budget Start Date
    9/4/2009 - 15 years ago
  • Budget End Date
    8/31/2010 - 14 years ago
  • Fiscal Year
    2009
  • Support Year
    3
  • Suffix
  • Award Notice Date
    8/31/2009 - 15 years ago
Organizations

ST-246 treatment of smallpox vaccine-related adverse events

DESCRIPTION (provided by applicant): Naturally occurring smallpox has been eradicated but remains a credible threat to the security of the United States due to its potential use as an agent of terror or biowarfare. Given that approximately 25% of the population is contraindicated to receive the vaccine due to direct risk of adverse events or the possibility of placing direct contacts at risk (23), the current smallpox vaccine is inadequate to protect the US population from smallpox. SIGA Technologies (SIGA) is currently conducting NDA-enabling activities seeking FDA approval for ST-246 as a post-exposure therapeutic for smallpox. SIGA is seeking to expand ST-246 indications for use to include it as an adjunct to smallpox vaccination to prevent or treat adverse events due to the vaccine. We and our collaborators have demonstrated in more than 30 animal studies that ST-246 is safe and very effective for the prevention or treatment of orthopoxvirus infection, including variola, the causative agent of smallpox. This suggested to us that ST-246 might also be used to prevent or treat adverse events due to the smallpox vaccine, a live vaccinia virus closely related to variola. We have demonstrated in immunocompetent mice (14) and monkeys that reactogenicity to the vaccine is reduced while protective immunity elicited by the vaccine is not affected. Further, in our Phase I studies, as reported in the Progress Report below, we have determined that ST-246 provides full protection from lethal poxvirus challenge in numerous murine models of immunodeficiency and that immunodeficient mice may be safely vaccinated if treated with ST-246 as an adjunct to the vaccine. Immunodeficient mice that are safely vaccinated are subsequently resistant to lethal challenge suggesting that remaining components of the immune system are able to mediate protection. ST-246 is a promising candidate for inclusion in the Strategic National Stockpile as a component of the Smallpox Response Plan to 1) provide protection from smallpox if an individual is exposed and 2) reduce the occurrence of adverse events due to vaccination. PUBLIC HEALTH RELEVANCE: The objective of this proposal is to advance ST-246 development as an adjunct to the smallpox vaccine through the pre-clinical development phase so that an Investigational New Drug (IND) application may be filed with the Food and Drug Administration upon completion of the proposed studies.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R44
  • Administering IC
    AI
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    999960
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:999960\
  • Funding Mechanism
    SBIR-STTR
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    SIGA TECHNOLOGIES, INC.
  • Organization Department
  • Organization DUNS
    932651516
  • Organization City
    CORVALLIS
  • Organization State
    OR
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    97333
  • Organization District
    UNITED STATES