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Completed Phase 2 Interventional Results available

A Study of Sipuleucel-T With Administration of Enzalutamide in Men With Metastatic Castrate-Resistant Prostate Cancer

ClinicalTrials.gov ID: NCT01981122

Public ClinicalTrials.gov record NCT01981122. 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 15, 2026, 1:52 PM 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 Randomized, Open-label, Phase 2 Study of Sipuleucel-T With Concurrent Versus Sequential Administration of Enzalutamide in Men With Metastatic Castrate-Resistant Prostate Cancer

Study identification

NCT ID
NCT01981122
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dendreon
Industry
Enrollment
52 participants

Conditions and interventions

Interventions

  • enzalutamide Drug
  • sipuleucel-T Biological

Drug · Biological

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
Aug 31, 2013
Primary completion
Jun 29, 2017
Completion
Jun 29, 2017
Last update posted
Oct 23, 2018

2013 – 2017

United States locations

U.S. sites
19
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Urological Associates of Southern Arizona, P.C. Tucson Arizona 85741
USC/Norris Comprehensive Cancer Center Los Angeles California 90033
The Urology Center of Colorado Denver Colorado 80211
Yale University School of Medicine New Haven Connecticut 06520
H. Lee Moffitt Cancer and Research Center Tampa Florida 33612
Uro Partners/ RMD Clinical Research Melrose Park Illinois 60160
Fort Wayne Medical Oncology and Hematology, Lutheran Hospital, Parkview Regional Medical Center Fort Wayne Indiana 46804, 46845
Johns Hopkins Medicine - Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21231
GU Research Network Omaha Nebraska 68130
North Shore Hematology/Oncology Associates, P.C. East Setauket New York 11733
Associated Medical Professionals of New York, PLLC Syracuse New York 13210
Raleigh Hematology Oncology Associates, D.B.A. Cancer Centers of North Carolina Raleigh North Carolina 27607
Cleveland Clinic - Taussig Cancer Institute Cleveland Ohio 44195
Thomas Jefferson University Philadelphia Pennsylvania 19107
Carolina Urologic Research Center Myrtle Beach South Carolina 29572
Urology Associates, PC Nashville Tennessee 37209
Urology of Virginia Virginia Beach Virginia 23462
Virginia Mason Medical Center, Virginia Mason Hospital Seattle Washington 98101
Northwest Medical Specialties, Rainier Physicians Tacoma Washington 98405

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 NCT01981122, 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 Oct 23, 2018 · Synced May 15, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01981122 live on ClinicalTrials.gov.

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