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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Hormone therapy
PhasePhase 2
DrugADT

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low13%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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