SBIR/STTR Research Award

HLS-Cardiac Safety AI Trained Human Heart and Micro Heart Model

Award identifier fb9d3496bde185f97716ef1a083a3b3d036252e68bd038ba40361ab7591a7acfAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$349,385

Program and phase

SBIR · Phase I

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
InvivoSciences, Inc.
Proposal award date
2018-09-01
Contract end date
2019-08-31
UEI
G5JDXMW3NSW3
Solicitation number
PA17-302
Topic code
NHLBI

Research abstract

HLSThe US FDA is considering to establish a new cardiac safety assessment approach defined by a new paradigm calledComprehensive in vitro Proarrhythmia AssayCIPAThe CIPA willassess drug effects on each cardiac ion channel type individually using a highthroughput assay ion channel assayscompute net effect on repolarization and risks for torsade pointesTdPusing a mathematical modelandconfirm the computational prediction by measuring the drug s effects on action potentials in induced pluripotent stem celliPSCderived human cardiac myocytesCMsThis paradigm shiftif successfulcould reduce the cost of cardiac safety analyses by replacing or lowering the requirement to perform an expensive$millionthorough QT study during clinical trialsProtecting consumers from drug induced arrhythmia and sudden deaths is a paramount importance for the regulators and pharmaceutical companies as well as lowing the cost of drug developmentMany cardiac safety scientistshoweverare skeptical about CIPA s approach since CMs derived from human iPSCs exhibit a poor excitation contraction coupling due to their immaturityIn additiona proposed CIPA mathematical model was developed to simulate electrophysiology of human adult CMsso there is a mismatch between experimental system and computational toolTo address these concernswe proposed three specific aims in twphases by following FastTrack SBIR processesPhase I feasibility Aimwill measure drug induced changes in AP and CaT using human adult heart slices isolated from human donorsHere we will confirm our successful handling and analyzing human adult heart sliceswhich will be based on a recently published protocol by our collaboratorDrIgor Efimovat George Washington UniversityAfter this validationwe will move on to perform the following two studiesAimCompare drug induced changes in AP and CaT in NuHearts generated from adult CMs and cardiac fibroblasts from same human donor heartsAimValidate and improve the computational models and train an artificial intelligence to predict cardiac safety risks of unknow compoundsAfter our successful completion proposed projectswe can establish an unprecedented cardiac safety assessment platform that can predict safety issues using a well trained AI without doing any experiments using human heart slices that are rarely accessible for most of the safety laboratories or biotech firms Because nearly one third of drug candidates fails to reach market due to its cardiac safety concernsa better safety assessment approach without increasing its cost is needed to improve productivity of pharmaceutical industryThe proposed project combines computational and experimental analyses of cardiac safety parameters using adult heart cells isolated from a donor heart and its stem cell derived heart muscle cells to build a better but cost effective cardiac safety assessment systemA successfully validated system enables drug developers to arcuately predict a new drug s cardiac safety profile by only running cost effective experiments using stem cell derived heart muscle cells that are accessible to many drug developers

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

15 SBIR/STTR records share this UEI (2004–2022). Reported award amounts total $12,363,639. 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

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