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Safety and Cognitive Function Study of EVP-6124 in Patients With Schizophrenia
NCT00968851 · View on ClinicalTrials.gov ↗
Study Summary
This study is being conducted to determine the safety and effect on cognitive function of two different doses of an investigational medication, EVP-6124, in individuals with schizophrenia who are on chronic stable atypical anti-psychotic therapy. In addition, behavioral and psychotic symptoms will be evaluated.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG EVP-6124
Study Locations (20)
Other
- — Arkhangelsk
- — Kazan'
- — Moscow
- — Moscow
- — Saint Petersburg
- — Stavropol
California
- Intergrated Medical and Behavioral Associates — Glendale
- Excell Research — Oceanside
- University of California, San Diego — San Diego
- Affiliated Research Institute — San Diego
- Schuster Medical Research Institute — Sherman Oaks
Illinois
- Uptown Research Institute — Chicago
- Alexian Brothers Behavioral Health — Hoffman Estates
Texas
- FutureSearch Clinical Trials, L.P. — Austin
- InSite Clinical Research — DeSoto
Florida
- Scientific Clinical Research, Inc. — North Miami
Maryland
- CBH Health, LLC — Rockville
New Jersey
- CRI Worldwide — Willingboro
South Carolina
- Carolina Clinical Trials, Inc. — Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 317 participants |
| Start Date | 2009-12 |
| Est. Completion | 2011-03 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00968851
The ClinicalTrials.gov registry entry for NCT00968851 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 317 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is FORUM Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Schizophrenia appearing as the primary indexed condition, and to 2 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: NCT00968851 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, California, Illinois. 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 NCT00968851 about?
NCT00968851 is a clinical study titled "Safety and Cognitive Function Study of EVP-6124 in Patients With Schizophrenia". This study is being conducted to determine the safety and effect on cognitive function of two different doses of an investigational medication, EVP-6124, in individuals with schizophrenia who are on chronic stable atypical anti-psychotic therapy. In addition, behavioral and psychotic symptoms will b...
What is the current status of trial NCT00968851?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 317 participants. The study started on 2009-12. Estimated completion is 2011-03.
What conditions does trial NCT00968851 study?
This clinical trial studies the following conditions: Schizophrenia, Cognition, Central Nervous System Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00968851?
The interventions under investigation include: Placebo (DRUG), EVP-6124 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00968851?
This trial is sponsored by FORUM Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00968851 being conducted?
This trial has 20 study locations across California, Florida, Illinois, Maryland, New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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