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A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer's Disease

What is this Study about?

The purpose of this study is to evaluate the efficacy and safety of KarXT + KarX-EC in adult participants with agitation related to Alzheimer's Disease.

What Will Happen in This Study?

Participant will take the study drug or placebo orally.
Planned duration of treatment is 14 weeks.

Who is Eligible to Participate in this Study?

Male or female participants aged 55 years of age to 90.
Must have a study partner
History of agitation due to AD.

Get in Touch About this Study

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Clinical Trial

Target Population

Person living with dementia, Person living with Alzheimer’s disease, Person at risk of Alzheimer's disease (AD) or living with pre-clinical AD

Study Location

In-Person
Ontario

Recruitment End Date

November 24, 2028
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