Low Cost, Rapid Molecular Diagnostic for Chlamydia and Gonorrhea at the Point-of-Care

Information

  • Research Project
  • 9466637
  • ApplicationId
    9466637
  • Core Project Number
    R43AI136161
  • Full Project Number
    1R43AI136161-01
  • Serial Number
    136161
  • FOA Number
    PA-16-302
  • Sub Project Id
  • Project Start Date
    1/1/2018 - 7 years ago
  • Project End Date
    12/31/2018 - 6 years ago
  • Program Officer Name
    DAVID, HAGIT S
  • Budget Start Date
    1/1/2018 - 7 years ago
  • Budget End Date
    12/31/2018 - 6 years ago
  • Fiscal Year
    2018
  • Support Year
    01
  • Suffix
  • Award Notice Date
    12/28/2017 - 7 years ago
Organizations

Low Cost, Rapid Molecular Diagnostic for Chlamydia and Gonorrhea at the Point-of-Care

PROJECT ABSTRACT The overall goal of this Phase I SBIR proposal to prove the feasibility of developing a rapid (<20 minute), CLIA-waived, fully automated, molecular diagnostic technology for the multiplexed detection of two sexually transmitted infections (STIs). ?Chlamydia trachomatis (CT) and ?Neisseria gonorrhoeae (NG) infections are the number one and two most commonly reported bacterial STIs, with an estimated 131 million and 78 million new cases annually of CT and NG, respectively worldwide. These infections are curable with antibiotics, however no rapid, accurate diagnostic test is available to inform clinical treatment decisions during the patient visit. Untreated infections lead to serious sequelae including pelvic inflammatory disease (PID) and its associated complications, such as ectopic pregnancy, infertility, and chronic pelvic pain. Furthermore, loss to follow-up is a significant problem with STI patients. Therefore, ?timely diagnosis using accurate diagnostics and early treatment is imperative?. Rapid, immunoassay based point-of-care (POC) tests for CT/NG fail to diagnose more than 50% of Chlamydia positive cases. Nucleic Acid Amplification Tests (NAATs) are the current gold standard for diagnosing CT/NG due to their high sensitivity and specificity. However the only FDA approved POC NAAT for CT/NG is expensive and takes more than 90 minutes for diagnosis. As such ?there is great need for an effective POC diagnostic test for CT/NG. ?Specific Aims: The Phase I deliverable of this project will be to validate a 20 minute POC NAAT for CT/NG in a clinical setting. In Aim 1, room temperature stable lyophilized reagents will be implemented on the device. In Aim 2, the sample-to-answer assay will be developed and validated for clinical samples. Finally in Aim 3, the POC test device for CT/NG will be evaluated by the clinician end-user, in an actual clinical setting, using freshly collected patient samples. With a projected cost-of-goods of under $5, our miniaturized molecular diagnostic device will address the need for affordable portable tests that enable accurate, detection and treatment of multiple STDs in lab-free, point of care settings.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R43
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    300000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:300000\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    NOVEL MICRODEVICES, LLC
  • Organization Department
  • Organization DUNS
    079691224
  • Organization City
    BALTIMORE
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    21202
  • Organization District
    UNITED STATES