drugset / Trial / NCT06651567

A Study to Assess the Efficacy and Safety of ITI-1284 in the Treatment of Agitation Associated With Alzheimer's Dementia

NCT06651567 ↗

Phase 2 Recruiting 320 enrolled Intra-Cellular Therapies, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, placebo-controlled, flexible-dose study of the efficacy, safety, and tolerability of ITI-1284 in patients with agitation associated with Alzheimer's dementia

Timeline

Start
2024-10-22
Primary completion
2027-12-28
Completion
2027-12-28

Drugs

EvaluationDrugModalityDoseRoute
Subject ITI-1284 Unknown 10 mg Other
Subject ITI-1284 Unknown 20 mg Other

Indications

No indication recorded.