72
Participants
Start Date
December 31, 2012
Primary Completion Date
June 21, 2017
Study Completion Date
June 21, 2017
OGX-427
OGX-427 started within 7 days of randomization, three loading doses of 600 mg IV within Week 1 if possible (up to 10 days of initiating treatment), followed by weekly doses of 800 mg IV
Abiraterone Acetate
Standard therapy: Abiraterone Acetate 1000 mg PO daily
Prednisone
Standard therapy: Prednisone 10-20 mg PO daily
Virginia Oncology Associates, Norfolk
Indiana University Melvin and Bren Simon Cancer Center, Indianapolis
IU Health Central Indiana Cancer Centers, Indianapolis
IU Health Goshen Hospital, Goshen
Northern Indiana Cancer Research Consortium, South Bend
IU Health Bloomington Hospital, Bloomington
Mayo Clinic, Rochester
University of New Mexico Cancer Center: Albuquerque, Albuquerque
Prostate Oncology Specialists, Inc., Marina del Rey
Dana Farber Cancer Institute, Boston
Alberta Health Services: Tom Baker Cancer Centre, Calgary
Cross Cancer Institute, Edmonton
BC Cancer Agency, Vancouver
Cancer Care Manitoba, Winnipeg
Juravinski Cancer Centre, Hamilton
Centre Hospitalier de l'Université de Montréal, Montreal
Collaborators (2)
Hoosier Cancer Research Network
OTHER
Achieve Life Sciences
INDUSTRY
Costantine Albany
OTHER