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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 Oct 24, 2026, 4:53 PM 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 29, 2016 (Actual)
Primary completion
Jan 30, 2019 (Actual)
Completion
Jan 30, 2019 (Actual)
Last update posted
Jun 29, 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 29, 2021 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02817906 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →