300 Participants Needed

Observational Study for Advanced Prostate Cancer

Recruiting at 2 trial locations
CK
Overseen ByCheryl Kefauver, RN
Age: 18+
Sex: Male
Trial Phase: Academic
Sponsor: University of Southern California
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to learn more about advanced prostate cancer that has spread beyond its original site. Researchers collect blood, urine, and tissue samples, along with information about treatment, diet, and quality of life, to improve future patient outcomes. Men diagnosed with advanced prostate cancer who are about to start a new treatment are ideal participants.

As a Phase 3 trial, this study represents the final step before FDA approval, offering participants the opportunity to contribute to a potentially groundbreaking treatment.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It is best to discuss this with the trial coordinators or your doctor.

Why are researchers excited about this trial?

Researchers are excited about the Longitudinal Advanced Prostate Cancer Cohort (LAPCC) trial because it takes a fresh approach by not testing a specific drug but by closely observing patients with advanced prostate cancer. Unlike traditional treatments like hormone therapy, chemotherapy, or surgery, this trial focuses on gathering detailed data from blood and urine samples, surveys, and medical records over time. The goal is to uncover patterns and insights that could lead to more personalized and effective treatment strategies in the future. This approach could significantly enhance our understanding of the disease and improve patient outcomes by tailoring treatments to individual needs.

Who Is on the Research Team?

AG

Amir Goldkorn, MD

Principal Investigator

University of Southern California

Are You a Good Fit for This Trial?

Inclusion Criteria

You are a male with metastatic prostate cancer set to commence systemic treatment, either for the first time or recurrently.
You may have previously taken part in clinical trials.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Observational

Patients undergo blood and urine sample collection, complete surveys, and have their medical records reviewed

Up to 5 years

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Non-Interventional Study

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: ObservationalExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Southern California

Lead Sponsor

Trials
956
Recruited
1,609,000+

National Cancer Institute (NCI)

Collaborator

Trials
14,080
Recruited
41,180,000+