SBIR/STTR Research Award

Functionally Mature Human Stem Cell Derived Cardiac Monolayers for Cardiotoxicity Testing

Award identifier 865b10a26d8887d6239249aa2e8f6ed45a5008f4c5395e4ca97e7cb70fd0a416Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$224,490

Program and phase

SBIR · Phase I

Award year

2017

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Cartox, LLC
Proposal award date
2017-09-01
Contract end date
2018-02-28
UEI
X2JKYW2D9EB3
Solicitation number
PA16-302
Topic code
NIEHS

Research abstract

Project Summary Abstract Cardiotoxicity is a common cause of pharmaceutical withdrawl from the market Ideally cardiotoxicity of a drug should occur early in the development process before extensive animal testing and clinical trials are performed The current pre clinical cardiotoxicity testing platform relies exclusively on an in vitro test that determines whether a drug blocks a single ionic current called hERG The FDA is calling for a change in the guidelines for in vitro pre clinical cardiotoxicity testing Specifically the FDA would like to include the use of human stem cell derived cardiomyocytes as part of the pre clinical screening process However the FDA has pointed out that the maturation state of human stem cell derived cardiomyocytes must be advanced and a high throughput electrophysiological testing platform must be developed before these cells can be used to replace the existing guidelines CARTOX LLC is developing cell culture plating technology that enables rapid maturation of human stem cell derived cardiomyocytes Preliminary data shows significant maturation of the structure and function of stem cell derived cardiomyocytes using patent pending cell culture plating technology The product that is in development is called MATURA MATURA enables rapid maturation of cells and also a platform for high throughput screening of drug effects on the human action potential The aims of this grant are To validate the predictive power of MATURA for cardiotoxicity and To validate the use of MATURA for study of long term effects of chronic drug treatment on human cardiac physiology Validation will be performed using FDA recommended panel of drugs with known risk high intermediate low for causing cardiotoxicity A phase II application will be competitive if the aims of this phase I SBIR application are completed Successful development of this product will enable the pharmaceutical and drug development industry to seriously address the Rs of animal usage reduction refinement replacement Project Narrative Public health is influenced by the development of new drug therapies to treat disease Safe and effective development of new drug therapies requires pre clinical in vitro cardiotoxicity testing in a model system relevant to the human condition The goal of this proposal is to develop a commercial product that will use functionally and structurally mature human stem cell derived cardiac monolayers for more efficient pre clinical safety screening

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

2 SBIR/STTR records share this UEI (2017–2019). Reported award amounts total $1,526,527. Reported amounts are not federal obligations.

Phases: Phase II, Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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