20
Participants
Start Date
February 28, 2014
Primary Completion Date
December 31, 2014
Study Completion Date
December 31, 2014
JNJ-42847922
Participants will receive suspension of JNJ-42847922 (10 mg, 20 mg, and 40 mg) orally on Day 1 of the appropriate treatment periods.
Placebo
Participants will receive placebo orally on Day 1 of the appropriate treatment periods.
Berlin
Leiden
Janssen Research & Development, LLC
INDUSTRY