NEXT-GEN Oral test for monitoring HIV/AIDS in Point-of-Care

Information

  • Research Project
  • 9142125
  • ApplicationId
    9142125
  • Core Project Number
    R44DE021672
  • Full Project Number
    2R44DE021672-02
  • Serial Number
    021672
  • FOA Number
    PA-15-269
  • Sub Project Id
  • Project Start Date
    8/15/2011 - 13 years ago
  • Project End Date
    8/31/2018 - 6 years ago
  • Program Officer Name
    GANNOT, GALLYA
  • Budget Start Date
    9/1/2016 - 8 years ago
  • Budget End Date
    8/31/2017 - 7 years ago
  • Fiscal Year
    2016
  • Support Year
    02
  • Suffix
  • Award Notice Date
    8/29/2016 - 8 years ago
Organizations

NEXT-GEN Oral test for monitoring HIV/AIDS in Point-of-Care

? DESCRIPTION (provided by applicant): NEXT-GEN Oral test for monitoring HIV/AIDS in Point-of-Care The ultimate goal of this project is to develop a new point-of-care test for acute HIV screening and therapeutic monitoring of HIV/AIDS in Point-of-care. The commercial product will be a compact sample-to-answer system with disposable cartridges, capable of achieving CLIA waiver. The test will be rapid (<20 minutes) and inexpensive (<$2). The test will measure HIV viral load and host response biomarkers in whole saliva using a microchip device. The device consists of a label-free, multiplexed immunoassay on a disposable microfluidic microchip coupled with a nanoplasmonic reader. Phase I R&D produced core innovations for the proposed product: candidate saliva biomarkers with >96% diagnostic accuracy for acute and unsuppressed HIV infection, and a prototype microfluidic device. These Phase I deliverables provide a solid foundation for the proposed Phase II activities. Key technical objective is to clinically validate the microchip device based on a high diagnostic accuracy for acute and unsuppressed HIV infection in a cross-section of HIV/AIDS patients and controls. SA1 will obtain N=195 saliva samples from 7 cohorts of HIV/AIDS patients and controls. SA2 will validate the diagnostic accuracy of the candidate biomarkers using the clinical saliva samples from SA1. The biomarkers will be measured using a high throughput saliva IHC immunoassay, and confirmed using orthogonal assays: Western blot and SRM mass spectroscopy. SA3 will adapt the prototype microchip device to measure HIV viral load and the candidate biomarkers in whole saliva. The new platform will be validated analytically based on high sensitivity, accuracy and reliability. Clinical validation will be demonstrated based on ?99% diagnostic accuracy for unsuppressed and acute HIV in clinical saliva samples from SA1. This milestone will provide key GO criteria for the commercial product development in Phase III. The proposed product has potential to radically improve the test and treat HIV strategy, help to reduce new infections, increase access to care and improve health outcomes for people living with HIV.

IC Name
NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH
  • Activity
    R44
  • Administering IC
    DE
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    434121
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    121
  • Ed Inst. Type
  • Funding ICs
    NIDCR:434121\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    GAIA MEDICAL INSTITUTE, LLC
  • Organization Department
  • Organization DUNS
    180402070
  • Organization City
    LA JOLLA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    920374616
  • Organization District
    UNITED STATES