OXALOBACTER FORMIGENES DIAGNOSTIC KIT DEVELOPMENT

Information

  • Research Project
  • 6647746
  • ApplicationId
    6647746
  • Core Project Number
    R44DK057500
  • Full Project Number
    5R44DK057500-03
  • Serial Number
    57500
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/2000 - 25 years ago
  • Project End Date
    8/31/2006 - 19 years ago
  • Program Officer Name
    GRETZ, ELIZABETH
  • Budget Start Date
    9/1/2003 - 22 years ago
  • Budget End Date
    8/31/2006 - 19 years ago
  • Fiscal Year
    2003
  • Support Year
    3
  • Suffix
  • Award Notice Date
    8/6/2003 - 22 years ago

OXALOBACTER FORMIGENES DIAGNOSTIC KIT DEVELOPMENT

DESCRIPTION (provided by applicant): Absence of Oxalobacter formigenes (Oxf) from the GI-tract is a risk factor for development of hyperoxaluria and calcium oxalate kidney stones. Recent data now indicate that patients with recurrent urolithiasis have a lower prevalence rate of Oxf in their stools than non-stone forming individuals. In addition, urinary oxalate levels are higher in non-colonized individuals as compared to colonized individuals. This indicates a clinical need for a test that can identify non-colonized individuals. Phase I of this grant resulted in the development of a reliable and rapid PCR ELISA-based microtiter plate assay for the detection of Oxf in human fecal samples. Pre-clinical performance data for the test (Le. its analytical sensitivity, analytical specificity, precision and reproducibility) were obtained as per the NCCLS guidelines. In Phase II of this project, we propose to complete the development of a production prototype of the XEntrix(TM) O. formigenes Monitor Kit. Analytical and clinical performance of the prototypic test kit will be determined in a multicentre clinical trial. The clinical studies have been designed not only to validate the test kit but also to strengthen the utility of Oxf determination as a diagnostic tool for the assessment of risk for calcium oxalate urolithiasis. By end of the proposed Phase II studies, we will have sufficient analytical and clinical performance data on this diagnostic kit to seek a pre-market approval under section 510K of the Food Drugs and Cosmetic Act, from the Center for Devices and Radiological Health.

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R44
  • Administering IC
    DK
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    387272
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
    NIDDK:387272\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    IXION BIOTECHNOLOGY, INC.
  • Organization Department
  • Organization DUNS
    957419716
  • Organization City
    ALACHUA
  • Organization State
    FL
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    32615
  • Organization District
    UNITED STATES