A Placebo-controlled Double-blind Parallel-Group Bayesian Adaptive Randomization Design and Dose Regimen-finding Study to Evaluate Safety Tolerability and Efficacy of BAN2401 in Subjects with Early Alzheimer's Disease
Martin Farlow, MD
Primary Investigator
Overview
The purpose of this research is to find out if the study drug has a benefit on a person?s cognitive status via a series of specialized cognitive tests. The purpose of this research is also to find out if this study drug is safe and well-tolerated in people with early Alzheimer?s disease.
Description
The purpose of this research is to find out if the study drug has a benefit on a person?s cognitive status via a series of specialized cognitive tests. The purpose of this research is also to find out if this study drug is safe and well-tolerated in people with early Alzheimer?s disease.
Eligibility
You may be eligible for this study if you meet the following criteria:
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Conditions:
Alzheimer's disease
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Age: Between 50 Years - 90 Years
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Gender: All