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COMPLETED Phase 2

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

NCT00694707 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Risperidone
  • DRUG Cariprazine

Study Locations (20)

California

  • Forest Investigative Site — Costa Mesa
  • Forest Investigative Site — Long Beach
  • Forest Investigative Site — Oceanside
  • Forest Investigative Site — Paramount
  • Forest Investigative Site — Riverside

Texas

  • Forest Investigative Site — Houston
  • Forest Investigative Site — Houston
  • Forest Investigative Site — Irving

Florida

  • Forest Investigative Site — Bradenton
  • Forest Investigative Site — Kissimmee

District of Columbia

  • Forest Investigative Site — Washington D.C.

Louisiana

  • Forest Investigative Site — Lake Charles

Maryland

  • Forest Investigative Site — Baltimore

Mississippi

  • Forest Investigative Site — Flowood

Missouri

  • Forest Investigative Site — Bridgeton

Trial Details

FieldValue
Enrollment Target 732 participants
Start Date 2008-06-30
Est. Completion 2009-08-31
Phase Phase 2

Sponsor

Forest Laboratories

32 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00694707

The ClinicalTrials.gov registry entry for NCT00694707 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 732 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Forest Laboratories, which has 32 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Schizophrenia appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00694707 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Texas, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00694707 about?

NCT00694707 is a clinical study titled "Safety and Efficacy of Cariprazine (RGH-188) in the Acute Exacerbation of Schizophrenia". 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.

What is the current status of trial NCT00694707?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 732 participants. The study started on 2008-06-30. Estimated completion is 2009-08-31.

What conditions does trial NCT00694707 study?

This clinical trial studies the following conditions: Schizophrenia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00694707?

The interventions under investigation include: Placebo (DRUG), Risperidone (DRUG), Cariprazine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00694707?

This trial is sponsored by Forest Laboratories, which has 32 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00694707 being conducted?

This trial has 20 study locations across California, District of Columbia, Florida, Louisiana, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial