drugset / Trial / NCT06540833

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

NCT06540833 ↗

Phase 2 Recruiting 370 enrolled Intra-Cellular Therapies, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, parallel-group, placebo-controlled, flexible-dose study evaluating the efficacy, safety, and tolerability of ITI-1284 compared with placebo in the treatment of psychosis in patients with AD.

Timeline

Start
2024-08-15
Primary completion
2028-09-30
Completion
2028-12-29

Drugs

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

Indications