An Efficacy and Safety Study of Sirukumab in Participants With Major Depressive Disorder

PHASE2CompletedINTERVENTIONAL
Enrollment

193

Participants

Timeline

Start Date

July 23, 2015

Primary Completion Date

May 22, 2018

Study Completion Date

May 22, 2018

Conditions
Depressive Disorder, Major
Interventions
DRUG

Sirukumab 50 mg

Participants will receive sirukumab 50 mg as subcutaneous injection on Day 1, 28 and 56.

DRUG

Placebo

Participants will receive matching placebo on Day 1, 28 and 56.

Trial Locations (46)

Unknown

Birmingham

Little Rock

Bellflower

Glendale

Lemon Grove

Orange

Santa Ana

Torrance

Wildomar

Atlanta

Decatur

Chicago

Edgewood

Baltimore

Grand Rapids

Lebanon

Brooklyn

New York

Staten Island

Columbus

Oklahoma City

Houston

Plano

Salt Lake City

Edmonton

Chatham

Hamilton

Toronto

Bełchatów

Bydgoszcz

Chełmno

Gorlice

Lublin

Karelia

Moscow

Nizny Novgorod

Rostov-on-Don

Saint Petersburg

Saratov

Saratov Region

Tomsk

Yaroslavl

Edinburgh

Glasgow

Oxford

Redruth

All Listed Sponsors
lead

Janssen Research & Development, LLC

INDUSTRY

NCT02473289 - An Efficacy and Safety Study of Sirukumab in Participants With Major Depressive Disorder | Biotech Hunter | Biotech Hunter