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Abstract Details

Multi-Modal Correlation Analyses From a Phase 2, Open-Label Study of NE3107 in Patients With Cognitive Decline Due to Degenerative Dementias
Aging, Dementia, and Behavioral Neurology
P7 - Poster Session 7 (8:00 AM-9:00 AM)
7-010
To determine correlations among changes in inflammatory markers, improvements in neuropsychological health, changes in brain metabolism and functional connectivity, and changes in patients’ daily abilities after NE3107 treatment.
Lowering chronic neuroinflammation may slow Alzheimer’s disease (AD) progression. An exploratory, 3-month, phase 2 trial of NE3107, an oral, anti-inflammatory molecule, enrolled 23 patients, 17 with mild cognitive impairment (MCI) to mild dementia [Mini-Mental State Examination (MMSE) scores ≥20] and 6 patients with moderate dementia (MMSE scores <20). In patients with MMSE ≥20, NE3107 treatment was associated with significant improvements in cognitive performance, including the AD assessment Scale-Cognitive Subscale 12 颅(ADAS-Cog12), trending improvements in biomarker levels, including tumor necrosis factor-α (TNF-α), significant improvements in the Global Rating of Change (GRC), and enhanced neurophysiological health. We assessed correlations between the anti-inflammatory effects and meaningful clinical outcomes. 
Eligible patients had a Clinical Dementia Rating score of 0.5 (MCI) or 1 (mild dementia). Clinicians, patients, and caregivers completed a GRC at study completion. Correlations between changes from baseline in cognitive function (ADAS-Cog12) and the key inflammatory biomarker (TNF-α) or patient global impression (GRC) were determined. Hypothesis-based examination of metabolic and functional brain imaging was initiated.
Patients had a mean age of 71.6 (SD=9.63) years and 15 (65%) were females. In patients with MMSE ≥20, reductions in TNF-α significantly correlated with improvements in ADAS-Cog12 scores (r=0.7; p=0.0077). Improvements in cognition, based on changes in ADAS-Cog12, significantly correlated with clinician-observed improvements in GRC outcomes (r=−0.52; p<0.05). Neuroimaging data suggest correlations with other study outcomes.
Correlations among improved cognitive function, reduced inflammation, and changes in the clinician-observed GRC (overall impression of patient’s abilities) were consistent with the hypothesized activities of NE3107.  Preliminary examination of metabolic and functional brain imaging supports hypothesis-based directional changes in accordance with the expected mechanism of action.
Authors/Disclosures
Joseph M. Palumbo, MD (BioVie)
PRESENTER
Dr. Palumbo has received personal compensation for serving as an employee of BioVie. An immediate family member of Dr. Palumbo has received personal compensation for serving as an employee of Merck Research Laboratories. Dr. Palumbo has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Stalicla SA. Dr. Palumbo has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Psychae Therapeutics Pty Ltd. Dr. Palumbo has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Phocus Pharmaceuticals Inc.. Dr. Palumbo has received personal compensation in the range of $0-$499 for serving as an officer or member of the Board of Directors for BioVie. Dr. Palumbo has or had stock in BioVie. An immediate family member of Dr. Palumbo has or had stock in Merck Research Laboratories. The institution of Dr. Palumbo has received research support from United States Department of Defense. Dr. Palumbo has received intellectual property interests from a discovery or technology relating to health care. Dr. Palumbo has received intellectual property interests from a discovery or technology relating to health care. Dr. Palumbo has received intellectual property interests from a discovery or technology relating to health care.
Jeffrey Zhang (Princeton Pharmatech LLC.) The institution of Jeffrey Zhang has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for BioVie.
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
Kaya G. Jordan, CRC (The Regenesis Project) Ms. Jordan has nothing to disclose.
Elisabeth Rindner (The Regenesis Project) Ms. Rindner has nothing to disclose.
No disclosure on file
No disclosure on file
No disclosure on file
Sheldon E. Jordan, MD (Neurological Associates of West Los Angeles) Dr. Jordan has stock in Synaptec Network.