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Clinical Trial Summary

The primary purpose of the study is to evaluate the safety and tolerability of emraclidine administered orally to healthy elderly participants in Part A (multiple ascending doses) and participants with dementia due to Alzheimer's disease (AD) in Part B.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05644977
Study type Interventional
Source Cerevel Therapeutics, LLC
Contact Cerevel Clinical Trial Support
Email cerevelclinicaltrials@cerevel.com
Status Recruiting
Phase Phase 1
Start date December 2, 2022
Completion date April 2025

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