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PREcision DIagnostics in Prostate Cancer Treatment (PREDICT)

Short Title: A032102


Enrollment Status: Recruiting

NCT #: A032102

Specialty Area: Oncology

Condition Studied: Prostate Cancer

Age Groups: Adult; Older Adult

Phase: II


Study Information

Summary / Purpose

The purpose of this study is to test whether genetic testing in prostate cancer is helpful in deciding which study treatment patients are assigned. This study will help the study doctors find out if this different approach is better, the same, or worse than the usual approach. To decide if it is better, the study doctors will be looking to see if assigning patients to targeted treatment based on genetic testing may help shrink or slow the cancer from growing.

Study Type: Interventional
Accepts Healthy Volunteers: No

Who Can Participate

Eligibility Criteria:
  • Adult males 18+ years of age
  • Confirmed progressive castration resistant prostate cancer
  • Must have measurable disease
  • No prior treatment with cabazitaxel plus carboplatin

What's Involved

Participation in the study will include:
  • Submitting tumor tissue from a previous surgery or biopsy for genetic testing to look for changes in the DNA and RNA of your cancer
  • Assignment to a treatment group based on the results of that genetic testing
  • Study treatment based on your assigned group, which may include chemotherapy given through a vein (IV), hormone therapy taken by mouth, a targeted therapy called valemetostat tosylate, or a radioligand therapy given through a vein that delivers radiation directly to tumor cells
  • Imaging with computed tomography (CT) scans, magnetic resonance imaging (MRI) scans, bone scans, prostate-specific membrane antigen (PSMA) positron emission tomography (PET) scans, and fludeoxyglucose (FDG) positron emission tomography (PET) scans
  • Sample collection for research, including blood samples during treatment
  • Completing questionnaires about your symptoms and side effects

Principal Investigator

Additional Information

Location: Renown Health, Office of Clinical Research
Address:

1500 E 2nd St. Reno, NV 89502

General Research: 775-982-3646
Oncology Research: 775-982-5050
Email: Renown-CRD@renown.org

Disclaimer: This listing gives you general information about the study and isn't part of the official consent process. If you decide to learn more, the research team will talk with you and check if you meet any additional requirements to join the study.

ER Wait Times

How are wait times calculated?

Our estimated ER wait times reflect the average time from check-in to being seen by a medical professional during triage, where patients are prioritized based on the severity of their condition.