15
Participants
Start Date
July 31, 2012
Primary Completion Date
September 30, 2012
Study Completion Date
September 30, 2012
Treatment A: abiraterone acetate
250 mg/day tablet administered orally on Day 1 of each treatment period.
Treatment B: abiraterone acetate
500 mg/day tablets administered orally on Day 1 of each treatment period.
Treatment C: abiraterone acetate
1000 mg/day tablets administered orally on Day 1 of each treatment period.
Beijing
Janssen Research & Development, LLC
INDUSTRY