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Spots Global Cancer Trial Database for A Study of Enzalutamide and LY3023414 in Men With Prostate Cancer

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Trial Identification

Brief Title: A Study of Enzalutamide and LY3023414 in Men With Prostate Cancer

Official Title: A Double-Blinded, Placebo-Controlled, Randomized Phase II Study of Enzalutamide With or Without the PI3 Kinase/mTOR Inhibitor LY3023414 in Men With Metastatic Castration Resistant Prostate Cancer

Study ID: NCT02407054

Study Description

Brief Summary: The main purpose of this study is to evaluate the safety and effectiveness of the study drug known as LY3023414 in combination with enzalutamide in men with prostate cancer.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Urology Centers of Alabama, P.C., Homewood, Alabama, United States

Highlands Oncology Group, Fayetteville, Arkansas, United States

Prostate Oncology Specialists, Marina Del Rey, California, United States

Sharp Memorial Hospital, San Diego, California, United States

Florida Cancer Specialists, Fort Myers, Florida, United States

Florida Cancer Specialists North, Saint Petersburg, Florida, United States

Florida Cancer Specialists East, West Palm Beach, Florida, United States

Ingalls Memorial Hospital, Harvey, Illinois, United States

Fort Wayne Oncology & Hematology, Fort Wayne, Indiana, United States

Indiana Cancer Pavilion, Indianapolis, Indiana, United States

Dana Farber Cancer Institute, Boston, Massachusetts, United States

Minnesota Oncology/Hematology PA, Minneapolis, Minnesota, United States

Urology Cancer Center, Omaha, Nebraska, United States

Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, United States

Garden State Urology, Morristown, New Jersey, United States

Delaware Valley Urology, Voorhees, New Jersey, United States

Associated Medical Professionals of NY, Syracuse, New York, United States

Oncology Hematology Care Inc, Cincinnati, Ohio, United States

Cleveland Clinic Foundation, Cleveland, Ohio, United States

Oregon Urology Institute, Springfield, Oregon, United States

Northwest Cancer Specialists PC, Tualatin, Oregon, United States

Urological Associates of Lancaster, Lancaster, Pennsylvania, United States

Univ of Pittsburgh Cancer Inst. (UPCI), Pittsburgh, Pennsylvania, United States

Carolina Urologic Research Center, Myrtle Beach, South Carolina, United States

Sarah Cannon Research Institute SCRI, Nashville, Tennessee, United States

Tennessee Oncology PLLC, Nashville, Tennessee, United States

Urology Associates, Nashville, Tennessee, United States

Southwestern Medical Center - Dallas, Dallas, Texas, United States

Texas Oncology-Baylor Charles A. Sammons Cancer Center, Fort Worth, Texas, United States

Texas Oncology-Memorial City, Houston, Texas, United States

US Oncology, The Woodlands, Texas, United States

University of Virginia Health System, Charlottesville, Virginia, United States

Virginia Cancer Specialists, Fairfax, Virginia, United States

Virginia Oncology Associates, Norfolk, Virginia, United States

Swedish Medical Center, Seattle, Washington, United States

Medical College of Wisconsin, Milwaukee, Wisconsin, United States

Contact Details

Name: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Affiliation: Eli Lilly and Company

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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