Condition: Prostatic Neoplasms, Castration-Resistant · Sponsor: Janssen Research & Development, LLC
The purpose of this study is to: a) establish the recommended phase 2 dose (RP2D) and to evaluate the antitumor activity and safety of niraparib combination therapies (Combinations 1 and 2) and b) to determine the relative bioavailability of niraparib and abiraterone acetate (AA) in combination (Combination 3) in participants with metastatic castration-resistant prostate cancer (mCRPC).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Urological Associates of Southern Arizona, P.C. | Tucson, Arizona, United States | — |
| The Urology Center of Colorado | Denver, Colorado, United States | — |
| Mayo Clinic - Division Of Hematology/oncology | Jacksonville, Florida, United States | — |
| First Urology, PSC | Jeffersonville, Indiana, United States | — |
| Chesapeake Urology Research Associates | Towson, Maryland, United States | — |
| Michigan Institute of Urology | Troy, Michigan, United States | — |
| New York Oncology Hematology | Albany, New York, United States | — |
| Memorial Sloan Kettering Cancer Center 1 | Harrison, New York, United States | — |
| Memorial Sloan Kettering Cancer Center | New York, New York, United States | — |
| Thomas Jefferson University | Philadelphia, Pennsylvania, United States | — |
| University of Pittsburgh Medical Center (UPMC) | Pittsburgh, Pennsylvania, United States | — |
| MUSC-Hollings Cancer Center | Charleston, South Carolina, United States | — |
+ 38 more locations — full list on the registry record.
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