Alzheimer's Disease Clinical Trial
Official title:
A Randomized, Double-Blind, Placebo Controlled, Multi-Center Study of the Pharmacodynamics/Efficacy, Safety, Tolerability, and Pharmacokinetics of 3 Fixed Dosages of MEM 3454 (5 mg, 15 mg, and 50 mg) in Patients With Mild to Moderate Alzheimer's Disease
The purpose of this study is to determine in an 8-week treatment study if MEM 3454 is a safe and effective treatment for patients with mild to moderate Alzheimer's disease.
Alzheimer's disease is the leading cause of dementia and one of the most common diseases of
the aging population. It is a chronic brain disease that involves gradual memory loss,
decline in the ability to perform routine tasks, disorientation, difficulty in learning,
loss of language skills, impairment of judgment, and personality changes in affected
individuals. The neurodegenerative nature of the disease eventually leads to the failure of
other organ systems and death.
A consistent and marked change in the brains of patients with AD is degeneration of the
cholinergic innervation in the hippocampus and cerebral cortex areas. The activity of
choline acetyl transferase (ChAT) is significantly reduced in these brain regions, and a
linear correlation is seen between the reduction in cortical ChAT activity and the progress
of dementia, indicating a progressive loss of cholinergic function.
Receptor selective nicotinic alpha-7 receptor agonists can modulate acetylcholine in
selective brain regions and contribute to symptomatic treatment of AD. MEM 3454 is a novel
nicotinic alpha-7 receptor selective partial agonist having serotonin type 3 (5-HT3)
receptor antagonist properties.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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