24
Participants
Start Date
September 28, 2018
Primary Completion Date
July 11, 2019
Study Completion Date
July 11, 2019
JNJ-63733657
Single ascending IV low, middle, and high dose of JNJ-63733657 will be administered in sequential cohorts. The progression to the next (higher) dose level is dependent on acceptable safety and tolerability profile of JNJ-63733657 obtained after dose administration of the current dose level. The length of time between dosing days of cohorts will be at least 14 days.
Placebo
Participants will receive matching placebo intravenously.
Souseikai Fukuoka Mirai Hospital, Fukuoka
Lead Sponsor
Janssen Pharmaceutical K.K.
INDUSTRY