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Completed Phase 2 Interventional Results available

Study Evaluating Vabicaserin in Subjects With Schizophrenia

ClinicalTrials.gov ID: NCT00563706

Public ClinicalTrials.gov record NCT00563706. 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 18, 2026, 12:26 AM 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, Risperidone-Referenced, Parallel-Group, Adaptive-Design Study of the Efficacy, Safety, and Tolerability of Vabicaserin (SCA-136) in Subjects With Acute Exacerbations of Schizophrenia

Brief summary

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

The primary purpose of this protocol is to establish the efficacy, safety, and tolerability of vabicaserin (SCA-136) using a once a day capsule in subjects with acute exacerbations of schizophrenia.

Study identification

NCT ID
NCT00563706
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
199 participants

Conditions and interventions

Conditions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
Male
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 2007 (Type not available)
Primary completion
Jun 2008 (Actual)
Completion
Jun 2008 (Actual)
Last update posted
Mar 20, 2014

2007 – 2008

United States locations

U.S. sites
32
U.S. states
15
U.S. cities
30
Facility City State ZIP Site status
Pfizer Investigational Site Little Rock Arkansas 72201 —
Pfizer Investigational Site Cerritos California 90703 —
Pfizer Investigational Site Escondido California 92025 —
Pfizer Investigational Site Garden Grove California 92845 —
Pfizer Investigational Site Glendale California 91206 —
Pfizer Investigational Site San Diego California 92103 —
Pfizer Investigational Site San Diego California 92123 —
Pfizer Investigational Site Torrance California 90502 —
Pfizer Investigational Site Washington D.C. District of Columbia 20016 —
Pfizer Investigational Site Aventura Florida 33180 —
Pfizer Investigational Site Hollywood Florida 33021 —
Pfizer Investigational Site Kissimmee Florida 34741 —
Pfizer Investigational Site Hoffman Estates Illinois 60169 —
Pfizer Investigational Site Indianapolis Indiana 46222 —
Pfizer Investigational Site Lake Charles Louisiana 70601 —
Pfizer Investigational Site Baltimore Maryland 21202 —
Pfizer Investigational Site Rockville Maryland 20850 —
Pfizer Investigational Site Hamilton New Jersey 08619 —
Pfizer Investigational Site Willingboro New Jersey 08046 —
Pfizer Investigational Site Cedarhurst New York 11516 —
Pfizer Investigational Site Holliswood New York 11423 —
Pfizer Investigational Site New York New York 10032 —
Pfizer Investigational Site Butner North Carolina 27509 —
Pfizer Investigational Site Oklahoma City Oklahoma 73103 —
Pfizer Investigational Site Philadelphia Pennsylvania 19131 —
Pfizer Investigational Site Austin Texas 78754 —
Pfizer Investigational Site Austin Texas 78756 —
Pfizer Investigational Site Bellaire Texas 77008 —
Pfizer Investigational Site DeSoto Texas 75115 —
Pfizer Investigational Site Houston Texas 77008 —
Pfizer Investigational Site Arlington Virginia 22201 —
Pfizer Investigational Site Portsmouth Virginia 23707 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00563706, 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 Mar 20, 2014 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00563706 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →