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Completed Phase 1 Interventional

A Safety Study of Abiraterone Acetate Administered in Combination With Docetaxel in Patients With Metastatic Castration-Resistant Prostate Cancer (mCRPC)

ClinicalTrials.gov ID: NCT01400555

Public ClinicalTrials.gov record NCT01400555. 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 16, 2026, 9:33 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 1b Safety Study of Abiraterone Acetate (JNJ-212082) and Docetaxel in Subjects With Metastatic Castration-Resistant Prostate Cancer (mCRPC)

Study identification

NCT ID
NCT01400555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Cougar Biotechnology, Inc.
Industry
Enrollment
22 participants

Conditions and interventions

Interventions

  • Cohort 1 Drug
  • Cohort 2 Drug
  • Cohort 3 Drug
  • Cohort 4 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
Aug 31, 2011
Primary completion
May 11, 2014
Completion
Feb 27, 2017
Last update posted
Mar 20, 2018

2011 – 2017

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Not listed Los Angeles California
Not listed New York New York
Not listed Madison Wisconsin

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 NCT01400555, 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 20, 2018 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01400555 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →