A Safety, Efficacy and Biomarker Study of JNJ-42847922 in Participants With Major Depressive Disorder

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

June 11, 2015

Primary Completion Date

January 4, 2016

Study Completion Date

January 4, 2016

Conditions
Major Depressive Disorder
Interventions
DRUG

JNJ-42847922

JNJ-428479, 20 milligram (mg) capsule, orally, once daily, at bedtime for 10 days in women of childbearing potential (WOCBP) or for 4 weeks in all other participants.

DRUG

Diphenhydramine

Diphenhydramine 25 mg capsule, orally, once daily, at bedtime for 10 days in women of childbearing potential (WOCBP) or for 4 weeks in all other participants.

DRUG

Placebo

Matching placebo (capsules containing neutral pellets), orally, once daily, at bedtime for 10 days in women of childbearing potential (WOCBP) or for 4 weeks in all other participants.

Trial Locations (7)

Unknown

Aalst

Brussels

Duffel

Berlin

Hamburg

Schwerin

Leiden

Sponsors
All Listed Sponsors
lead

Janssen-Cilag International NV

INDUSTRY