Viewing Study NCT00057239



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00057239
Status: COMPLETED
Last Update Posted: 2010-10-04
First Post: 2003-03-27

Brief Title: An 8 Week Depression Study In Adults Diagnosed With Major Depressive Disorder
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: A Multi-Center Randomized Double-Blind Parallel-Group Placebo-Controlled Fixed-Dose Study Evaluating the Efficacy Safety and Tolerability of Two Doses 20mg and 60mg of a Once-Daily Oral Formulation of GW353162 in Subjects With Major Depressive Disorder for a Treatment Period of Eight Weeks
Status: COMPLETED
Status Verified Date: 2010-10
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: A Placebo Controlled Study Evaluating Efficacy Safety and Tolerability of Radafaxine in Patients with Major Depressive Disorder MDD
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