drugset / Trial / NCT07011745

A Phase 3 Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer's Disease

NCT07011745 ↗

Phase 3 Recruiting 426 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2025-07-16
Primary completion
2028-11-03
Completion
2028-11-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Trospium Small molecule — —
Subject Xanomeline Small molecule — —

Indications