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Completed Phase 2 Interventional

Safety and Cognitive Function Study of EVP-6124 in Patients With Schizophrenia

ClinicalTrials.gov ID: NCT00968851

Public ClinicalTrials.gov record NCT00968851. 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 20, 2026, 2:24 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 12-Week Phase 2 Study of Two Different Doses of an Alpha-7 Nicotinic Acetylcholine Receptor Agonist(EVP-6124)or Placebo in Schizophrenia Subjects on Chronic Stable Atypical Anti-Psychotic Therapy

Brief summary

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

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.

Study identification

NCT ID
NCT00968851
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
FORUM Pharmaceuticals Inc
Industry
Enrollment
317 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 55 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
Dec 2009 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Mar 2011 (Actual)
Last update posted
Apr 25, 2014

2009 – 2011

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
13
Facility City State ZIP Site status
Intergrated Medical and Behavioral Associates Glendale California 91204 —
Excell Research Oceanside California 92056 —
University of California, San Diego San Diego California 92103 —
Affiliated Research Institute San Diego California 92108 —
Schuster Medical Research Institute Sherman Oaks California 91403 —
Scientific Clinical Research, Inc. North Miami Florida 33161 —
Uptown Research Institute Chicago Illinois 60640 —
Alexian Brothers Behavioral Health Hoffman Estates Illinois 60169 —
CBH Health, LLC Rockville Maryland 20850 —
CRI Worldwide Willingboro New Jersey 20850 —
Carolina Clinical Trials, Inc. Charleston South Carolina 29407 —
Vanderbilt Psychiatric Hospital Nashville Tennessee 37212-8645 —
FutureSearch Clinical Trials, L.P. Austin Texas 78756 —
InSite Clinical Research DeSoto Texas 75115 —

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00968851, 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 Apr 25, 2014 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00968851 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →