Computational Tools for Research in Neuroscience, Behavioral Science and Mental H

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$2,406,347.00
Award Year:
2012
Program:
STTR
Phase:
Phase II
Contract:
2R42NS055475-04A1
Award Id:
n/a
Agency Tracking Number:
R42NS055475
Solicitation Year:
2012
Solicitation Topic Code:
NINDS
Solicitation Number:
PA11-097
Small Business Information
MOLECULAR NEUROIMAGING, LLC (Currently Molecular Neuroimaging, L.l.c.)
60 TEMPLE STREET, SUITE 8A, NEW HAVEN, CT, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
20285081
Principal Investigator:
GEORGE ZUBAL
(203) 401-4300
gzubal@mnimaging.com
Business Contact:
JACK MARIOTTI
(203) 401-4351
jmariotti@mnimaging.com
Research Institution:
UNIV OF TX SW MED CTR-DALLAS

5323 HARRY HINES BLVD.
DALLAS, TX, 75390-9105
() -
Nonprofit college or university
Abstract
DESCRIPTION (provided by applicant): We propose to develop a software package to automatically evaluate a subject's beta amyloid PET scan (using either C11-PIB, F18-florbetaben, or F18-florbetapir, F18-flutemetamol) by normalizing the subject's scan, masking away non-gray matter tissue (without relying on co-registered MRI scans), placing standardized ROIs onto the transverse slices, and reporting SUVr values in separate brain areas referenced to the cerebellar gray matter. Our goal is that this analysis package ultimately would be FDA-510(k) approved and distributed to hospitals and clinics (and pharmaceutical companies), as a commercial product, to aid in the evaluation and diagnosis of patients. Through the use of such a validated and standardized analysis package, new radio-tracers can be objectively compared for their accuracy in quantitating beta amyloid in the brain, and more importantly, new therapies can be objectively and quantitatively evaluated for their efficacy in preventing or removing beta amyloid for each patient, on a personalized individual basis. An important portion of the testing, user interface evaluation, and ADER's report generation utility and clinical application will be conducted in a subaward under the supervision of Dr. Michael Devous within the Nuclear Medicine Center at the UT Southwestern Medical Center, Dallas, Texas. At MNI, New Haven, we will continue to test and evaluate ADER in house within our Radio-tracer Evaluation Program (RTEP) program, where we continue to test potential new beta amyloid PET and SPECT imaging agents, while clinically evaluating subjects by our in-house neurologists and support staff. The potential benefit to society is considerable since an ADER analysis package would provide a quantitative biomarker analysis method for Alzheimer's disease progression for individualized therapy efficacy. Alzheimer's disease (AD) is associated with significant morbidity and a useful marker and/or brain scan analysis package, like this proposed ADER, would add to our understanding of AD disease progression and provide objective assessment of neuroprotective and restorative therapies. This fully automated image processing will also allow for fewer subjects to be studied (with the same clinical power) in clinical trials using new PET and SPECT radioligands. As new tracers and therapies are developed, ADER would co-evolve with these studies into an optimized image analysis method for diagnosing, staging and treating Alzheimer's disease. PUBLIC HEALTH RELEVANCE: Evaluation of Radiotracers (ADER) Project Narrative We propose to develop an automated package for analysis of beta-amyloid accumulation in Alzheimer's patients' brains which can be easily implemented by pharmaceutical companies for therapeutic drug discovery, aswell as in a clinical setting, for high quality quantitative PET (and SPECT) imaging assessments. This analysis will remove subjectivity in the determination of the imaging outcome measure and permit a reproducible evaluation of new Alzheimer's radio- tracers' imaging potential. ADER can be used to test the efficacy of new Alzheimer's therapies in which FDA Phase II tested radiotracers are used as surrogate biomarkers. Our validated image processing package is highly relevant to the ongoing search for new diagnostics and treatments since it will serve as a new medical device (as defined by the FDA), which will improve the way in which medical care is delivered to Alzheimer's patients.

* information listed above is at the time of submission.

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