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Terminated Phase 2 Interventional Results available

Double Blind, Randomized, 3 Week Inpatient Study To Evaluate The Safety & Efficacy Of PF-02545920 Compared With Placebo

ClinicalTrials.gov ID: NCT00570063

Public ClinicalTrials.gov record NCT00570063. 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 21, 2026, 10:07 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 Phase 2, Multicenter, Double-blind, Randomized, Fixed Dose, Parallel Group, 3-week Inpatient Treatment Study To Evaluate The Safety, Efficacy And Pharmacokinetics Of Pf-02545920 Compared With Placebo In The Treatment Of Acute Exacerbation Of Schizophrenia

Brief summary

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

To assess the efficacy and safety of an investigational compound PF-02545920 for the treatment of schizophrenia. PF-02545920 will be more effective than placebo in reducing symptoms associated with schizophrenia.

Study identification

NCT ID
NCT00570063
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
35 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 99 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
Nov 2007 (Actual)
Primary completion
Feb 18, 2008 (Actual)
Completion
Feb 18, 2008 (Actual)
Last update posted
Dec 20, 2017

2007 – 2008

United States locations

U.S. sites
10
U.S. states
4
U.S. cities
7
Facility City State ZIP Site status
California Clinical Trials Medical Group, Inc. Glendale California 91206 —
Glendale Adventist Medical Center Glendale California 91206 —
Telecare-Cresta Loma Lemon Grove California 91945 —
California Clinical Trials Medical Group Paramount California 90723 —
LaPaz Geropsychiatric Center Paramount California 90723 —
California Clinical Trials Medical Group San Diego California 92123 —
Connecticut Mental Health Center-Yale University, Clinical Neuroscience Research Unit New Haven Connecticut 06519 —
CRI Worldwide, LLC Willingboro New Jersey 08046 —
St. Anthony Hospital Oklahoma City Oklahoma 73101 —
IPS Research Company Oklahoma City Oklahoma 73103 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00570063, 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 Dec 20, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00570063 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →