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Completed Phase 2 Interventional Results available

3-arm Study of Abiraterone Acetate Alone, Abiraterone Acetate Plus Degarelix, a GnRH Antagonist, and Degarelix Alone for Patients With Prostate Cancer With a Rising PSA or a Rising PSA and Nodal Disease Following Definitive Radical Prostatectomy

ClinicalTrials.gov ID: NCT01751451

Public ClinicalTrials.gov record NCT01751451. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 14, 2026, 4:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, 3-arm Study of Abiraterone Acetate Alone, Abiraterone Acetate Plus Degarelix, a GnRH Antagonist, and Degarelix Alone for Patients With Prostate Cancer With a Rising PSA or a Rising PSA and Nodal Disease Following Definitive Radical Prostatectomy

Study identification

NCT ID
NCT01751451
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Memorial Sloan Kettering Cancer Center
Other
Enrollment
124 participants

Conditions and interventions

Interventions

  • Abiraterone acetate Drug
  • Abiraterone acetate plus degarelix Drug
  • Degarelix Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 17, 2012
Primary completion
Sep 27, 2020
Completion
Sep 27, 2020
Last update posted
Nov 18, 2021

2012 – 2020

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
Northwestern University, Feinberg School of Medicine Chicago Illinois 60611
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21287
Karmanos Cancer Institute, Wayne State University Detroit Michigan 48201
Urology Cancer Center and GU Research Network Omaha Nebraska 68130
Memoral Sloan Kettering Cancer Center Basking Ridge New Jersey
Cancer Institute of New Jersey New Brunswick New Jersey 08903
Memorial Sloan Kettering Cancer Center @ Suffolk Commack New York 11725
Memorial Sloan Kettering West Harrison Harrison New York 10604
NorthShore University Health System Long Island City New York
Memorial Sloan Kettering Cancer Center New York New York 10065
Weill Cornell Medical Center New York New York
Memorial Sloan Kettering at Mercy Medical Center Rockville Centre New York
Memoral Sloan Kettering Cancer Center at Phelps Sleepy Hollow New York 10591
University of North Carolina Chapel Hill North Carolina 27514
Duke University Medical Center Durham North Carolina 27701
Oregon Health & Science University Knight Cancer Institute Portland Oregon 97239

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01751451, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 18, 2021 · Synced May 14, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01751451 live on ClinicalTrials.gov.

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