Condition: Prostate Cancer · Sponsor: AstraZeneca
The purpose of the study is to demonstrate superiority of Saruparib (AZD5305) relative to placebo added to a standard radiation therapy (RT) + androgen deprivation therapy (ADT) regimen by assessment of metastases-free survival in participants with high-risk and very high-risk localised/locally advanced prostate cancer with a breast cancer gene mutation (BRCAm).
This description comes directly from the study's public registry record.
AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
Always discuss trial participation with your own doctor first.
| Research Site | Phoenix, Arizona, United States | Recruiting |
| Research Site | Tucson, Arizona, United States | Withdrawn |
| Research Site | La Jolla, California, United States | Recruiting |
| Research Site | La Jolla, California, United States | Recruiting |
| Research Site | Los Angeles, California, United States | Recruiting |
| Research Site | San Diego, California, United States | Recruiting |
| Research Site | San Luis Obispo, California, United States | Recruiting |
| Research Site | Lakewood, Colorado, United States | Recruiting |
| Research Site | Hialeah, Florida, United States | Recruiting |
| Research Site | Jacksonville, Florida, United States | Recruiting |
| Research Site | Tallahassee, Florida, United States | Withdrawn |
| Research Site | Tampa, Florida, United States | Recruiting |
+ 330 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06952803