Project Grant R44AG079694
- This Project Grant award from the National Institute on Aging (CFDA 93.866 - Aging Research) will provide $794,981 to the University of California, San Diego (UCSD) to investigate the use of blood-brain barrier permeability and brain microstructure as biomarkers for predicting and monitoring amyloid-related imaging abnormalities (ARIA) and treatment outcomes in Alzheimer's disease patients prescribed anti-amyloid immunotherapies. The study aims to integrate advanced MRI techniques into...
- This Cooperative Agreement award of $3,310,951 from the National Institute of Neurological Disorders and Stroke (NINDS), under the Extramural Research Programs in the Neurosciences and Neurological Disorders (CFDA 93.853) program, aims to develop and validate advanced in vivo MRI techniques, analytical tools, and plasma biomarkers to characterize the vascular pathophysiology underlying Amyloid-Related Imaging Abnormalities (ARIA) in a longitudinal cohort. The research team at New York University...
- This Project Grant award of $766,133 from the National Institute on Aging (CFDA 93.866 - Aging Research) supports research to understand the mechanisms leading to amyloid-related imaging abnormalities (ARIA) that can occur with anti-amyloid immunotherapy for Alzheimer's disease. The research aims to: Determine the elimination pathway and clearance mechanism for chimeric anti-amyloid antibodies (ChAbs) in Alzheimer's disease mouse models. Examine how ARIA events develop in Alzheimer's disease...
- The General Hospital Corporation (MGH) Research Management Division was awarded a $458,585 Project Grant from the National Institute on Aging (NIA) under the Aging Research program (CFDA 93.866) to develop a method for detecting autoantibodies against beta-amyloid in serum as a potential biomarker for Alzheimer's disease (AD). The 2-year project aims to investigate the use of small molecule compounds called CRANAD-XS to differentially tune the binding between beta-amyloid and its...
- This R01 project grant award from the National Institute on Aging (CFDA 93.866 Aging Research) provides $6,467,513.00 to Brigham & Women's Hospital Inc. to continue funding for the Ante-Amyloid Treatment of Alzheimer's Disease (A3) Trial and the Alzheimer Plasma Extension (APEX) Study. The A3 Trial is testing low-dose lecanemab, an amyloid-removing monoclonal antibody, in participants with intermediate brain amyloid levels to determine the optimal window for efficacy and safety of...
- This federal Project Grant award from the National Institute on Aging (CFDA 93.866 - Aging Research) provides $699,964 to Turing Medical Technologies Inc. (doing business as Nous Imaging, Inc.) to develop "Universal FIRMM", a real-time motion tracking and monitoring solution for all MRI imaging sequences. The objective is to create a software system compatible with any MRI scanner that can detect and reduce patient motion during MRI scans, with a specific focus on improving MRI...
- This $481,250 Project Grant was awarded by the National Institute on Aging (CFDA 93.866 Aging Research) to Vanderbilt University Medical Center (VUMC) on September 1, 2024. The award supports the development of an innovative, non-invasive MRI imaging technique to assess membrane lipid properties in Alzheimer's disease (AD). The key objectives are to: 1) verify the relationship between the MRI nuclear Overhauser enhancement (NOE) signal and lipid properties using reconstituted phospholipid...
- This $4.46 million project grant from the National Institute on Aging, part of the Department of Health and Human Services, supports research under the Aging Research program (CFDA 93.866) to develop a new in vivo magnetic resonance imaging biomarker for early detection of Alzheimer's disease neurodegeneration. Specifically, the awardee, Washington University, will utilize quantitative gradient recalled echo MRI techniques to identify two types of hippocampal tissue in preclinical and mild...
- This $1,531,729 Cooperative Agreement award from the National Institute of Neurological Disorders and Stroke (NINDS) under the Extramural Research Programs in the Neurosciences and Neurological Disorders (CFDA 93.853) aims to conduct a multimodal analysis of amyloid-related imaging abnormalities (ARIA) in Alzheimer's disease. The University of Pittsburgh will refine postmortem 7T MRI brain imaging methods, optimize co-registration between pre- and post-mortem MRI and histological data, and...
- This Project Grant award from the National Institute on Aging (CFDA 93.866 - Aging Research) provides $455,009 to The General Hospital Corporation (doing business as Massachusetts General Hospital) to develop a novel [18F]-labeled amphiphilic PET probe that can cross the blood-brain barrier and track CD206+ microglia/macrophages in Alzheimer's disease. The goal is to create a non-invasive imaging method to detect anti-inflammatory M2-like microglia and macrophages, which play a key role in...
QUANTIFICATION OF ARIA DURING THE TREATMENT OF ALZHEIMER'S PATIENTS - PROJECT SUMMARY/ABSTRACT ALZHEIMER'S DISEASE IS CHARACTERIZED BY B-AMYLOID DEPOSITS AND NEUROFIBRILLARY TANGLES PRECEDING NEURONAL LOSS AND COGNITIVE DECLINE. THE OVERALL GOAL OF THIS PROPOSAL IS TO DETECT AND QUANTIFY TREATMENT-RELATED CHANGES AND ABNORMALITIES IN ALZHEIMER PATIENTS' BRAINS USING MR IMAGES WHILE PATIENTS ARE UNDERGOING AMYLOID CLEARING DRUG TREATMENT. WE WILL DEVELOP AND VALIDATE THE LESION DETECTION AND QUANTIFICATION SOFTWARE AND DEPLOY IT AS A CLINICALLY USABLE TOOL. CURRENT DETECTION OF ARIA LESIONS DEPENDS ON VISUAL DETECTION BY TRAINED RADIOLOGISTS. IN RECENT YEARS, MULTIPLE AMYLOID DEPOSIT MODIFYING DRUGS HAVE BEEN DEVELOPED AND USED IN TRIALS WITH ALZHEIMER'S DISEASE PATIENTS. DURING THESE DRUG TRIALS, IT IS NOT UNCOMMON THAT SOME PATIENTS DEVELOPED IMAGING ABNORMALITIES IN THE BRAIN AND CLINICAL SYMPTOMS. THESE AMYLOID-RELATED IMAGING ABNORMALITIES (ARIA) MANIFEST AS INTRACEREBRAL HEMORRHAGE (ARIA-H), AND VASOGENIC EDEMA (ARIA-E). WITH THE RECENT FDA APPROVAL OF AMYLOID-TARGETING MONOCLONAL ANTIBODY ADUCANUMAB IN ALZHEIMER'S DISEASE, BRAIN IMAGING HAS BECOME AN INDISPENSABLE TOOL TO MONITOR THE PATIENTS' BRAINS DURING THERAPY. THE CURRENT RECOMMENDATION ON USE OF THE AMYLOID CLEARING DRUG ADUCANUMAB IS TO HAVE MRIS PRIOR TO INITIATING THERAPY, DURING THE TITRATION OF THE DRUG, AND AT ANY TIME THE PATIENT HAS SYMPTOMS SUGGESTIVE OF ARIA. IT IS RECOMMENDED TO HAVE DOSE INTERRUPTION OR TREATMENT DISCONTINUATION FOR SYMPTOMATIC ARIA AND MODERATE-SEVERE ARIA. IN ADDITION, CEREBRAL AMYLOID ANGIOPATHY (CAA) PATIENTS ALSO EXPERIENCE ARIA-LIKE LESIONS IN THEIR BRAINS AND MRI IS THE RECOMMENDED IMAGING MODALITY TO MONITOR THE CAA PROGRESSION. ONE WOULD EXPECT THAT IN THE NEAR FUTURE AMYLOID DEPOSIT MODIFYING DRUGS WILL BE USED IN AUTOSOMAL DOMINANT AD, OR OTHER AMYLOID RELATED DISEASES SUCH AS LEVY BODY DEMENTIA CONCOMITANT WITH AMYLOID BETA ACCUMULATION, OR DOWN SYNDROME WHERE AMYLOID PLAQUES AND SYMPTOMS OF DEMENTIA DEVELOPS LATER IN MIDLIFE OF THE PATIENTS. THEREFORE, A TREATMENT MONITORING BRAIN IMAGING SOFTWARE WILL HAVE AN IMPORTANT ROLE IN TERMS OF PATIENT CARE IN A WIDER SET OF DISEASE ENTITIES WHERE PATIENTS ARE GIVEN AMYLOID CLEARING DRUGS.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $0 | 9/11/25 | ||
| Not listed | $932.7k | 6/4/25 | ||
| Not listed | $932.7k | 6/4/25 | ||
| Not listed | $295.8k | 7/24/24 | ||
| Not listed | $295.8k | 7/24/24 |