Development of RLIP76 protein as a Radiation Countermeasure

Information

  • Research Project
  • 8663174
  • ApplicationId
    8663174
  • Core Project Number
    R44AI081356
  • Full Project Number
    5R44AI081356-05
  • Serial Number
    081356
  • FOA Number
    PA-10-123
  • Sub Project Id
  • Project Start Date
    5/1/2009 - 16 years ago
  • Project End Date
    5/31/2017 - 8 years ago
  • Program Officer Name
    RIOS, CARMEN I.
  • Budget Start Date
    6/1/2014 - 11 years ago
  • Budget End Date
    5/31/2017 - 8 years ago
  • Fiscal Year
    2014
  • Support Year
    05
  • Suffix
  • Award Notice Date
    5/14/2014 - 11 years ago
Organizations

Development of RLIP76 protein as a Radiation Countermeasure

DESCRIPTION (provided by applicant): There remains a critical need for medicines that can counteract the toxic effects of radiation exposure. Terapio is developing a recombinant protein, RLIP76, for use as a radioprotectant for workers, military personnel, or civilians that are either in imminent danger of radiation exposure, or have already been exposed. In research carried out at the University of Texas at Arlington, RLIP76 delivered in a liposome was discovered to have significant effects in protecting mice exposed to otherwise lethal doses of radiation, even if the proteoliposome was administered as late as 24 hours after exposure. Terapio was formed to develop and commercialize the protein for use as a radioprotectant. The company was awarded a Phase I SBIR from which exploratory efficacy studies were carried out confirming significant efficacy of the RLIP76 proteoliposome by a variety of routes of administration, including subcutaneous and intramuscular injection, a marked advantage for therapy that has to be delivered in the field. Now the company is applying for a Phase II SBIR to continue that work and carry out the studies necessary to file for an IND. Specifically, the goals of the current application are: 1.) to develop the necessary assays for IND-enabling studies and to verify the proposed tissue-level mechanism of action to the degree required by the FDA; 2.) to perform IND-enabling studies and 3.) to carry out animal safety and toxicokinetic studies in two species (rat and primate) as required by the FDA. Successful completion of these goals will position the company to file an IND in preparation for performing pivotal animal efficacy and human safety studies to support a subsequent New Drug Application.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R44
  • Administering IC
    AI
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    1000000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:1000000\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    TERAPIO
  • Organization Department
  • Organization DUNS
    806143207
  • Organization City
    AUSTIN
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    787385411
  • Organization District
    UNITED STATES