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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
The purpose of this study is to test the safety and effectiveness of talnetant vs. risperidone vs. placebo in reducing positive and negative symptoms in acutely psychotic schizophrenia patients.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
GSK Investigational Site
Little Rock, Arkansas, United States
GSK Investigational Site
Anaheim, California, United States
GSK Investigational Site
Cerritos, California, United States
GSK Investigational Site
Garden Grove, California, United States
GSK Investigational Site
Glendale, California, United States
GSK Investigational Site
National City, California, United States
GSK Investigational Site
Oceanside, California, United States
GSK Investigational Site
Pico Rivera, California, United States
GSK Investigational Site
Rosemead, California, United States
GSK Investigational Site
San Diego, California, United States
Start Date
December 1, 2004
Primary Completion Date
October 1, 2005
Completion Date
October 1, 2005
Last Updated
February 15, 2013
275
Estimated participants
Talnetant
DRUG
Lead Sponsor
GlaxoSmithKline
NCT07455929
NCT06740383
Data Source & Attribution
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