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Completed Phase 2 Interventional

Study Of Talnetant Versus Placebo And Risperidone In Schizophrenia

ClinicalTrials.gov ID: NCT00103727

Public ClinicalTrials.gov record NCT00103727. 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 Jul 23, 2026, 2:58 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 Multicenter, Double-Blind, Double-Dummy, Placebo-Controlled, Randomized, Parallel Group Evaluation of the Efficacy and Safety of a Fixed-Dose of Talnetant Versus Placebo Versus Risperidone in Subjects With Schizophrenia

Study identification

NCT ID
NCT00103727
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
282 participants

Conditions and interventions

Conditions

Interventions

  • Talnetant Drug
  • placebo Other
  • risperidone Other

Drug · Other

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 30, 2004
Primary completion
Sep 30, 2005
Completion
Sep 30, 2005
Last update posted
Apr 28, 2015

2004 – 2005

United States locations

U.S. sites
22
U.S. states
11
U.S. cities
21
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72201
GSK Investigational Site Anaheim California 92805
GSK Investigational Site Cerritos California 90703
GSK Investigational Site Garden Grove California 92845
GSK Investigational Site Glendale California 91206
GSK Investigational Site National City California 91950
GSK Investigational Site Oceanside California 92056
GSK Investigational Site Pico Rivera California 90660
GSK Investigational Site Rosemead California 91770
GSK Investigational Site San Diego California 92123
GSK Investigational Site San Diego California 92126
GSK Investigational Site Upland California 91786
GSK Investigational Site Washington D.C. District of Columbia 20016
GSK Investigational Site North Miami Florida 33161
GSK Investigational Site Atlanta Georgia 30308
GSK Investigational Site Oak Brook Illinois 60523
GSK Investigational Site St Louis Missouri 63118
GSK Investigational Site Clementon New Jersey 08021
GSK Investigational Site Philadelphia Pennsylvania 19131
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Irving Texas 75062
GSK Investigational Site Richmond Virginia 23294

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 NCT00103727, 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 28, 2015 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00103727 live on ClinicalTrials.gov.

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