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Completed Phase 3 Interventional Results available

Efficacy and Safety of Iloperidone Compared With Placebo and Active Control in Subjects With Acute Schizophrenia

ClinicalTrials.gov ID: NCT00254202

Public ClinicalTrials.gov record NCT00254202. 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 Jun 25, 2026, 4:55 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- and Active-controlled, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of Iloperidone in Schizophrenic Patients in Acute Exacerbation Followed by a Long-term Treatment Phase.

Study identification

NCT ID
NCT00254202
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
593 participants

Conditions and interventions

Conditions

Interventions

  • Iloperidone Drug
  • Ziprasidone Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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 17, 2005
Primary completion
Sep 25, 2006
Completion
Mar 20, 2007
Last update posted
Dec 12, 2024

2005 – 2007

United States locations

U.S. sites
33
U.S. states
14
U.S. cities
31
Facility City State ZIP Site status
Vanda Investigational Site Little Rock Arkansas 72211
Vanda Investigational Site Anaheim California 92805
Vanda Investigational Site Cerritos California 90703
Vanda Investigational Site Garden Grove California 92845
Vanda Investigational Site Glendale California 91206
Vanda Investigational Site Los Angeles California 90048
Vanda Investigational Site National City California 91950
Vanda Investigational Site Oceanside California 92056
Vanda Investigational Site Paramount California 90723
Vanda Investigational Site Pico Rivera California 90660
Vanda Investigational Site San Diego California 92123
Vanda Investigational Site San Diego California 92126
Vanda Investigational Site San Diego California 92161
Vanda Investigational Site Santa Ana California 92705
Vanda Investigational Site Upland California 91786
Vanda Investigational Site Bradenton Florida 34208
Vanda Investigational Site Fort Lauderdale Florida 33308
Vanda Investigational Site Maitland Florida 32751
Vanda Investigational Site Atlanta Georgia 30308
Vanda Investigational Site Augusta Georgia 30912
Vanda Investigational Site Hoffman Estates Illinois 60194
Vanda Investigational Site Lake Charles Louisiana 70601
Vanda Investigational Site Rockville Maryland 20850
Vanda Investigational Site Saint Charles Missouri 63301
Vanda Investigational Site St Louis Missouri 63118
Vanda Investigational Site Clementon New Jersey 08021
Vanda Investigational Site Brooklyn New York 11203
Vanda Investigational Site Cincinnati Ohio 45267
Vanda Investigational Site Philadelphia Pennsylvania 19131
Vanda Investigational Site Austin Texas 78756
Vanda Investigational Site Houston Texas 77057
Vanda Investigational Site Irving Texas 75062
Vanda Investigational Site Richmond Virginia 23229

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 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00254202, 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 12, 2024 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00254202 live on ClinicalTrials.gov.

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