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Completed Phase 2 Interventional Results available

Safety and Efficacy of Cariprazine (RGH-188) in the Acute Exacerbation of Schizophrenia

ClinicalTrials.gov ID: NCT00694707

Public ClinicalTrials.gov record NCT00694707. 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 19, 2026, 3:16 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

Evaluation of the Safety and Efficacy of RGH-188 in the Acute Exacerbation of Schizophrenia

Brief summary

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

This is a study to evaluate the safety, efficacy, and tolerability of cariprazine (RGH-188) relative to placebo in adult patients (18-60 years of age) with acute exacerbation of schizophrenia.

Study identification

NCT ID
NCT00694707
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Forest Laboratories
Industry
Enrollment
732 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 60 Years
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
Jun 30, 2008 (Actual)
Primary completion
Aug 31, 2009 (Actual)
Completion
Aug 31, 2009 (Actual)
Last update posted
Jun 12, 2019

2008 – 2009

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Forest Investigative Site Costa Mesa California 92626 —
Forest Investigative Site Long Beach California 90813 —
Forest Investigative Site Oceanside California 92056 —
Forest Investigative Site Paramount California 90723 —
Forest Investigative Site Riverside California 92506 —
Forest Investigative Site Washington D.C. District of Columbia 20016 —
Forest Investigative Site Bradenton Florida 34208 —
Forest Investigative Site Kissimmee Florida 34741 —
Forest Investigative Site Lake Charles Louisiana 70601 —
Forest Investigative Site Baltimore Maryland 21202 —
Forest Investigative Site Flowood Mississippi 39232 —
Forest Investigative Site Bridgeton Missouri 63044 —
Forest Investigative Site Cincinnati Ohio 45219 —
Forest Investigative Site Charleston South Carolina 29405 —
Forest Investigative Site Memphis Tennessee 28117 —
Forest Investigative Site Houston Texas 77008 —
Forest Investigative Site Houston Texas 77021 —
Forest Investigative Site Irving Texas 75062 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00694707, 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 12, 2019 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00694707 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →