SBIR/STTR Research Award

Rapid STEMI Fibrinolysis for Underserved Populations

Award identifier e619060aebcaee2e9015dec90c60cdaf4d2d55bcf3f47da9ccddfd24ead67735Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$396,934

Program and phase

SBIR · Phase I

Award year

2014

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Pulse Therapeutics, Inc.
Proposal award date
2014-08-28
Contract end date
2017-05-31
UEI
RL7DEN9VENV1
Solicitation number
EB13-002
Topic code
NIMHD

Research abstract

DESCRIPTION provided by applicant Coronary heart disease CHD accounts for every of deaths in the United States US with acute incidences estimated at M annually Of these up to are classified as ST elevation myocardial infarction STEMI in which a clot blocks a coronary artery leading to a change in the ECG ST wave Because the heart muscle rapidly dies time to reperfusion is critical While current CHD annual indirect costs are high they are projected to further increase from $ B in to $ B by Early percutaneous coronary intervention PCI remains the standard of care in the US However PCI has not shown to be of benefit to STEMI patients living in rural communities due to increased transportation times Efforts to expand PCI to rural communities have largely failed due to new PCI centers only being established in urban regions As a result andgt of transferred STEMI patients do not receive PCI therapy within the recommended min from first medical contact resulting in significantly higher mortality and greater patient costs Given that over M people live in geographically remote or rural communities andgt miles from a PCI center it is estimated that andgt k STEMI victims will remain without timely access to PCI each year While clot dissolving drugs are effective most physicians remain uncomfortable with their elevated bleeding risk and sub PCI recanalization rates Fundamentally thrombolytic drugs are limited in their effectiveness due to their inability to rapidly diffuse to clot in the occluded vessel due to poor fluid dynamics Pulse Therapeutics Inc andapos s PTIandapos s patented and clinically tested technology has overcome this limitation in a way that dramatically accelerates drug delivery to a clot by using non drug attached magnetite particles controlled by a magnetic cart in the emergency department However by attaching the FDA approved drug tenecteplase TNK to PTIandapos s magnetite particles the technology promises substantially faster clot lysis while eliminating associated bleeding risks with therapy deliverable in both the community hospital and ambulance settings Unfortunately this strategy likely faces an expensive FDA combination product regulatory pathway PTIandapos s objective is to demonstrate dramatic improvements in fibrinolysis by attaching TNK to magnetite particles In Phase I PTI will attempt to develop a optimally sized magnetite particle with the best performing TNK coating conjugated to the magnetite surface collect data on candidate particleandapos s clot lysis rates in vitro optimize a software algorithm for automated particle collection develop an ECG signal filtering system to enable the use of the technology without affecting electrocardiographic waveforms and conduct investigations evaluating lysis efficacy and hemorrhage risks in preclinical animal models The proposed technology has dramatic implications for rural STEMI treatment and will address the American Heart Associationandapos s concern that andquot Where you live should not determine whether you live andquot PUBLIC HEALTH RELEVANCE Pulse Therapeutics Inc intends to substantially improve accelerate and expand care to remote underserved populations for ST elevation myocardial infarction STEMI by attaching tenecteplase TNK to its magnetically controlled particles Of the andgt k STEMI events seen in the US each year of the victims are in rural communities andgt min away from an urban area which results in substantially inferior care due to persistent transfer times for percutaneous coronary intervention By extending its patented proven and clinically evaluated technology Pulse Therapeutics hopes to destroy blood clots faster and more reliably while substantially reducing TNK associated hemorrhage risks thereby greatly accelerating therapy for those victims without timely access to qualified medical facilitie

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

6 SBIR/STTR records share this UEI (2014–2021). Reported award amounts total $4,854,288. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.