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Study details
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Abiraterone/Prednisone + Standard ADT vs Standard ADT for Prostate Cancer Patients With PSMA-Positive Conventional Imaging Negative Pelvic Lymphadenopathy

University of Nebraska
NCT IDNCT07237269ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

140

Study length

about 7 years

Ages

30+

Sex

Male only

Locations

1 site in NE

What this study is about

This trial is testing whether a treatment with abiraterone and prednisone, plus standard hormone therapy, is better than standard hormone therapy alone for prostate cancer patients whose lymph nodes show signs of the disease using a special imaging test. The goal is to see if this new treatment leads to longer survival without the cancer coming back compared to the usual treatment.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Hormone therapy

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

hormone therapy, abiraterone, prednisone

Drug routes

oral

Endpoints

Secondary: Evaluate 5-year overall survival, Evaluate and compare patient-reported symptom outcomes in both arms from 3 months to 2 years post-ADT. (FACT-P), Evaluate and compare patient-reported symptom outcomes in both arms from 3 months to 2 years post-ADT. (IPSS), Evaluate local progression-free survival (i.e., failure-free survival excluding biochemical failure)., Evaluate locoregional progression-free survival (i.e., failure-free survival excluding biochemical failure)., Toxicity in both arms from 3 months to 2 years post-ADT.

Procedures

radiation

Body systems

Oncology