Start Date
May 31, 2016
Primary Completion Date
May 31, 2022
Study Completion Date
May 31, 2022
Abiraterone Acetate
This is an observational study and participants will not receive any intervention as a part of this study. All prospective participants who will be prescribed abiraterone acetate tablets 250 milligram (mg) treatment based on independent clinical judgment and as per locally approved prescribing information will be enrolled in the PMS. Participants will be exclusively observed for safety.
Bangalore
Delhi
New Delhi
Lead Sponsor
Johnson & Johnson Private Limited
INDUSTRY