142
Participants
Start Date
April 29, 2015
Primary Completion Date
September 26, 2018
Study Completion Date
April 16, 2020
LY3023414
Administered orally
Enzalutamide
Administered orally
Placebo
Administered orally
Associated Medical Professionals of NY, Syracuse
Univ of Pittsburgh Cancer Inst. (UPCI), Pittsburgh
Urological Associates of Lancaster, Lancaster
Virginia Cancer Specialists, Fairfax
University of Virginia Health System, Charlottesville
Virginia Oncology Associates, Norfolk
Carolina Urologic Research Center, Myrtle Beach
Florida Cancer Specialists East, West Palm Beach
Florida Cancer Specialists North, St. Petersburg
Florida Cancer Specialists, Fort Myers
Urology Centers of Alabama, P.C., Homewood
Sarah Cannon Research Institute SCRI, Nashville
Tennessee Oncology PLLC, Nashville
Urology Associates, Nashville
Cleveland Clinic Foundation, Cleveland
Oncology Hematology Care Inc, Cincinnati
Fort Wayne Oncology & Hematology, Fort Wayne
Medical College of Wisconsin, Milwaukee
Minnesota Oncology/Hematology PA, Minneapolis
Ingalls Memorial Hospital, Harvey
Urology Cancer Center, Omaha
Highlands Oncology Group, Fayetteville
Southwestern Medical Center - Dallas, Dallas
Texas Oncology-Baylor Charles A. Sammons Cancer Center, Fort Worth
Texas Oncology-Memorial City, Houston
US Oncology, The Woodlands
Comprehensive Cancer Centers of Nevada, Las Vegas
Prostate Oncology Specialists, Marina del Rey
Sharp Memorial Hospital, San Diego
Northwest Cancer Specialists PC, Tualatin
Oregon Urology Institute, Springfield
Swedish Medical Center, Seattle
Indiana Cancer Pavilion, Indianapolis
Dana Farber Cancer Institute, Boston
Garden State Urology, Morristown
Delaware Valley Urology, Voorhees Township
Sarah Cannon
INDUSTRY
Eli Lilly and Company
INDUSTRY