SBIR/STTR Research Award

Rapid oral test for Influenza A+B diagnostics

Award identifier bfad2b227aac63d8af526c63d7420885a53ff608cb714bb8874c86601f076915Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$971,053

Program and phase

SBIR · Phase II

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
GAIA MEDICAL INSTITUTE, LLC, THE
Proposal award date
2016-09-01
Contract end date
2019-08-31
UEI
H95RP93WA9V5
Solicitation number
PA18-591
Topic code
NIDCR

Research abstract

PROJECT SUMMARY Rapid oral test for Influenza A B diagnostics The goal of this project is to develop rapid oral test for diagnostics of influenza A BInfluenza is a highly contagious viral infection of the respiratory tract that causes disease in millions of people globallyInfluenza outbreaks occur each year and the associated costs in the US exceed $billion annuallyRecentlyeffective antiviral therapy for influenza became availableThe therapy needs to be initiated withindays of symptom onset to be effectivewhich raised the importance of influenza testing in Point of carePOCThe gold standard for objective diagnostics of influenza infection is a laboratory RT PCR assayRapid Influenza Diagnostic TestsRIDTprovide solution for POC diagnosticsRIDTs are disposable immunoassays that detect Influenza A and B antigens in andltminRIDT have major weaknesses limiting their clinical utilityiThe nasopharyngeal swabNPSspecimen is invasive to obtainiiThe sensitivity is lowThere is unmet need for a noninvasive RIDT with high sensitivityThe ultimate goal of this project is to develop oral RIDT that will use whole saliva specimenKey advantages of oral RIDT compared to NPS RIDTNoninvasive sampleSaliva can be collected easilysafely and noninvasivelyThis is a major advantage over NPSin particular for children and seniorsHigh sensitivityOral RIDT has potential for a higher sensitivity than the NPS RIDT because the concentration of detectable influenza antigen in saliva can be increased by lysing saliva epithelial cells to release cell associated viral proteinsThe proposed Phase I study will provide a proof of concept for influenza A immunoassay in saliva sampleSAwill show analytical feasibility of measuring major influenza A antigensNPHA and NAin whole salivaSAwill leverage existing saliva samples from patients diagnosed with influenza A to show feasibility of detecting influenza A antigens in clinical salivaExpected OutcomesThe proposed Phase I SBIR research will demonstrate the feasibility of oral test for influenza diagnosticsThe scientific premise is strong based on recent discovery of high influenza viral load in in patient saliva and buccal cellsDemonstration of technical feasibility in SAwill provide GO criteria for development of a commercial oral RIDT for Influenza A B in Phase IIIf successfulthe project has potential for high impact by providing noninvasivehighly sensitive oral test for influenza diagnostics that will enable immediateeffective treatment decisions in POCThe proposed oral influenza test has a strong commercial potential based on no competition and existing team of proven industry partners PROJECT NARRATIVE Rapid oral test for Influenza A B diagnostics Influenza is a highly contagious infectious disease that affects millions of people each year and can cause severe illness or death in people at risk such as children and seniorsThe goal of this project is to develop oral influenza test that will help patients to get rapid result and effective treatment in doctor s office or community pharmacy

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

7 SBIR/STTR records share this UEI (2011–2022). Reported award amounts total $7,719,388. Reported amounts are not federal obligations.

Phases: Phase I, Phase II – Direct to Phase II, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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