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Terminated Phase 3 Interventional Results available

ITI-007 for the Treatment of Agitation in Patients With Dementia, Including Alzheimer's Disease

ClinicalTrials.gov ID: NCT02817906

Public ClinicalTrials.gov record NCT02817906. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 5:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy and Safety of ITI-007 in the Treatment of Agitation in Patients With Dementia, Including Alzheimer's Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a randomized, double-blind, placebo-controlled study comparing the efficacy and safety of ITI-007 versus placebo administered orally once daily in the treatment of agitation in patients with dementia, including Alzheimer's disease.

Study identification

NCT ID
NCT02817906
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Intra-Cellular Therapies, Inc.
Industry
Enrollment
177 participants

Conditions and interventions

Eligibility (public fields only)

Age range
55 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 28, 2016
Primary completion
Jan 29, 2019
Completion
Jan 29, 2019
Last update posted
Jun 28, 2021

2016 – 2019

United States locations

U.S. sites
26
U.S. states
11
U.S. cities
26
Facility City State ZIP Site status
Not listed Sun City Arizona
Not listed Little Rock Arkansas
Not listed Rogers Arkansas
Not listed Costa Mesa California
Not listed Glendale California
Not listed Irvine California
Not listed Lemon Grove California
Not listed Long Beach California
Not listed Oceanside California
Not listed Riverside California
Not listed Santa Ana California
Not listed Hallandale Florida
Not listed Hialeah Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Suwanee Georgia
Not listed Honolulu Hawaii
Not listed Las Vegas Nevada
Not listed Berlin New Jersey
Not listed Marlton New Jersey
Not listed Toms River New Jersey
Not listed Brooklyn New York
Not listed Staten Island New York
Not listed Centerville Ohio
Not listed Dayton Ohio
Not listed San Antonio Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02817906, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 28, 2021 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02817906 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →