Viewing Study NCT00300963



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Last Modification Date: 2024-10-26 @ 9:23 AM
Study NCT ID: NCT00300963
Status: COMPLETED
Last Update Posted: 2013-02-15
First Post: 2006-03-07

Brief Title: Effect Of Talnetant Versus Risperidone Versus Placebo On Psychotic Symptoms In Schizophrenic Patients
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

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
Status: COMPLETED
Status Verified Date: 2013-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None