SBIR/STTR Research Award

CM-65, a Targeted Contrast Agent for Cardiac Magnetic Resonance Perfusion Imaging

Award identifier 6a8224d8d9154af70110ad9d8dfc21b2fd5d22a33028fe056939fb4a4962517cAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$857,523

Program and phase

SBIR · Phase II

Award year

2015

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
COLLAGEN MEDICAL LLC
Proposal award date
2015-05-15
Contract end date
2018-04-30
UEI
GJLBDQT8K757
Solicitation number
PA12-088
Topic code
NHLBI

Research abstract

DESCRIPTION provided by applicant Assessment of myocardial perfusion is a gatekeeper diagnostic exam that has high sensitivity for identifying individuals with ischemic heart disease Millions of perfusion studies are performed annually in the US using a stress rest paradigm with a radioactive tracer followed by nuclear imaging While this is an effective exam it involves delivering a dose of ionizing radiation to the patient and the spatial resolution of the technique s rather low which limits detection of smaller or subendocardial perfusion defects Cardiovascular magnetic resonance imaging CMR is considered a competitive first line test for common indications such as the evaluation of ischemic heart disease CMR involves no radiation and has an order of magnitude higher spatial resolution than nuclear techniques CMR can assess both myocardial perfusion and infarction with independent techniques in a single session However current CMR assessment of perfusion involves adenosine stress of the patient while in the scanner and rapid imaging to assess perfusion of first pass of the MR contrast agent With this project we aim to develop a technique that allows high quality prolonged visualization of myocardial perfusion using CM a novel MR imaging agent targeted to type I collagen We have shown in preliminary studies in pigs that CM can be administered during stress hyperemia and identify perfusion defects in the heart even after stress is ceased In Phase I of the study we will develop a clinically feasible CM stress perfusion protocol in a large animal model that can be directly adapted for use in humans In Phase II we will test the optimized clinically feasible CM protocol across a range of flow reduction with and without myocardial infarction in large animal models We will also address several of the safety and pharmacokinetic studies required for IND submission Together these data will form the basis for an IND submission for clinical testing of CM enhanced MR in the context of ischemic heart disease Assessment of myocardial perfusion is critical to identify individuals with ischemic heart disease This project involves developing a new magnetic resonance imaging probe to obtain high resolution perfusion maps without the use of ionizing radiation

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

20 SBIR/STTR records share this UEI (2012–2024). Reported award amounts total $15,782,674. 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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