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Completed Phase 2 Interventional Results available

Concurrent vs. Sequential Sipuleucel-T & Abiraterone Treatment in Men With Metastatic Castrate Resistant Prostate Cancer

ClinicalTrials.gov ID: NCT01487863

Public ClinicalTrials.gov record NCT01487863. 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 Jul 22, 2026, 10:34 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 Randomized, Open-label, Phase 2 Trial of Sipuleucel-T With Concurrent Versus Sequential Administration of Abiraterone Acetate Plus Prednisone in Men With Metastatic Castrate Resistant Prostate Cancer (mCRPC)

Study identification

NCT ID
NCT01487863
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dendreon
Industry
Enrollment
69 participants

Conditions and interventions

Interventions

  • sipuleucel-T Biological
  • abiraterone acetate Drug

Biological · 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
Nov 30, 2011
Primary completion
Apr 30, 2016
Completion
May 31, 2016
Last update posted
Mar 18, 2019

2011 – 2016

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
UCSD Medical Center - La Jolla La Jolla California 92037
Moores UCSD Cancer Center La Jolla California 92093
Cancer Center Oncology Medical Group La Mesa California 91942
UCSD Medical Center - Hillcrest San Diego California 92103
Medical Oncology Associates - SD San Diego California 92123
Sharp Rees-Stealy San Diego California 92123
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California 94115
The Urology Center of Colorado Denver Colorado 80211
Georgetown University Medical Center - Lombardi Cancer Center Washington D.C. District of Columbia 20007
Indiana University Indianapolis Indiana 46202
Mid Atlantic Urology Associates, Mid Atlantic Clinical Research Greenbelt Maryland 20770
GU Research Center, LLC Omaha Nebraska 68130
NYU Clinical Cancer Center, NYU Langone Medical Center New York New York 10016
The Mount Sinai Medical Center New York New York 10029
Associated Medical Professionals of NY, PLLC Oneida New York 13421
Associated Medical Professionals of New York, PLLC Syracuse New York 13210
Providence Cancer Center Oncology and Hematology Care Portland Oregon 97213
Carolina Urologic Research Center Myrtle Beach South Carolina 29572
Urology Associates, P.C. Nashville Tennessee 37209
Urology of Virginia Virginia Beach Virginia 23462
Virginia Mason Medical Center Seattle Washington 98101

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 NCT01487863, 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 Mar 18, 2019 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01487863 live on ClinicalTrials.gov.

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