A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed Dose Study Evaluating the Efficacy and Safety of Orvepitant in Subjects With Major Depressive Disorder

PHASE2TerminatedINTERVENTIONAL
Enrollment

328

Participants

Timeline

Start Date

March 1, 2009

Primary Completion Date

June 1, 2010

Study Completion Date

June 16, 2010

Conditions
Depressive Disorder, Major
Interventions
DRUG

orvepitant

Neurokinin-1 (NK-1) antagonist

OTHER

placebo

inactive placebo to match orvepitant 30 and 60 mg dosage forms

Trial Locations (20)

10029

GSK Investigational Site, New York

10467

GSK Investigational Site, The Bronx

32751

GSK Investigational Site, Maitland

32806

GSK Investigational Site, Orlando

33161

GSK Investigational Site, North Miami

34208

GSK Investigational Site, Bradenton

35216

GSK Investigational Site, Birmingham

43623

GSK Investigational Site, Toledo

53562

GSK Investigational Site, Middleton

66212

GSK Investigational Site, Overland Park

85251

GSK Investigational Site, Scottsdale

90210

GSK Investigational Site, Beverly Hills

91007

GSK Investigational Site, Arcadia

91786

GSK Investigational Site, Upland

91950

GSK Investigational Site, National City

98104

GSK Investigational Site, Seattle

02868

GSK Investigational Site, Lincoln

L7R 4E2

GSK Investigational Site, Burlington

K1C 1T1

GSK Investigational Site, Ottawa

M5G 2C4

GSK Investigational Site, Toronto

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT00880399 - A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed Dose Study Evaluating the Efficacy and Safety of Orvepitant in Subjects With Major Depressive Disorder | Biotech Hunter | Biotech Hunter