SBIR/STTR Research Award

The Diagnostic Utility of the in-vitro "Provoked" D dimer test in patients with suspected pulmonary embolism

Award identifier 83d83a5be4fabc9f44a8e2a8c6763a559e449664ee1029da75dc0db11e64a219Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$148,864

Program and phase

STTR · Phase I

Award year

2019

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
AUGDIMER, LLC
Proposal award date
2019-09-20
Contract end date
2020-08-31
UEI
JKD4KNWPF9W4
Solicitation number
PA18-575
Topic code
NHLBI

Research abstract

Project SummaryThe D Dimer assay is the current diagnostic standard to exclude patients of VTE due to its high sensitivityHoweverD Dimer levels are commonly elevated in patients without thromboembolismleading to poor specificity and poor positive predictive valuePPVDue to the lack of a robust diagnostic tool for VTEwe propose a novel advancement upon current DDimer testing which improves specificity through the addition of thrombolytics in vitro to increase the degradation of fibrin multimers present from the incomplete digestion of the in vivo fibrin rich clotThis increases the D Dimer signal in instances of a true clotThe elevation in theprovokedD DimerPDDsignal in comparison to the baselineor Standard D DimerSDDcan be used to improve the specificity and PPV of the D Dimer assayOur patented D Dimer test appears to move the field towards these goals but requires further study aimed at understanding the characteristic and efficacy of commercially available thrombolyticsThe PDD assay is a simplerapidand economical detection method for thromboembolism which improves specificity and PPV while maintaining high SDD sensitivityOur PDD assay has U Sand Europe patents which coverof the $billion worldwide market and we are currently seeking to commercialize our discoveryOur discussions with hemostasis diagnosis companies has lead us to two top prioritiesDetermine optimal incubation time and concentration needed for commercially available thrombolytics to establish their role in performing the provoked D dimer methodologyTo evaluate the test characteristics of all commercially available thrombolytic agents in effecting the new provoked D dimer methodology so that the most durable and effective agent can be utilizedTo accomplish thiswe are applying for the Small Business Technology TransferSTTRPhaseaward to stimulate clinical application of our patented technological innovationDrRobinson is from an underrepresented minorityAfrican Americanwhere the STTR mission is to foster and encourage participation in innovation and entrepreneurship in this groupClinicallywe anticipate with our PDD a true screening test will now be developed for patients with potential thromboembolismThe potential areas which will be impacted in the future are cryptogenic strokeatrial fibrillation risk stratificationscreening of immobile individualsand defining thromboembolic risk in cardiomyopathic patientsProject Narrative Venous ThromboembolismVTEis a major cause of disability and death in the United StatesWe plan to optimize a new blood test which promises to simplify the diagnosis of VTE in humansIf goals of our project are achievedit will result in reduced death and morbidity from venous thromboembolic diseases

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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