38
Participants
Start Date
July 11, 2017
Primary Completion Date
December 6, 2017
Study Completion Date
December 6, 2017
JNJ-64041575
All participants will receive a single oral dose of 1,000 mg JNJ-64041575 (4\*250 mg tablets) on Day 1.
APEX GmbH, München
CRS Clinical Research Services Kiel, Kiel
Janssen Pharmaceutica N.V., Belgium
INDUSTRY