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Terminated Phase 2 Interventional Results available

OGX-427 in Metastatic Castrate-Resistant Prostate Cancer With Prostate-Specific Antigen Progression While Receiving Abiraterone

ClinicalTrials.gov ID: NCT01681433

Public ClinicalTrials.gov record NCT01681433. 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 Oct 21, 2026, 3:20 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

The Pacific Clinical Trial: A Randomized Phase II Study Evaluating OGX-427 in Patients With Metastatic Castrate-Resistant Prostate Cancer (MCRPC)Who Have Prostate-Specific Antigen (PSA) Progression While Receiving Abiraterone: Hoosier Oncology Group GU12-159

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase II study has been designed to evaluate the anti-tumor effects of adding OGX-427 to continuing abiraterone acetate and prednisone treatment in men with metastatic castrate-resistant prostate cancer (MCRPC) who have prostate-specific antigen (PSA) progression

Study identification

NCT ID
NCT01681433
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Costantine Albany
Other
Enrollment
72 participants

Conditions and interventions

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 2012 (Actual)
Primary completion
Jun 21, 2017 (Actual)
Completion
Jun 21, 2017 (Actual)
Last update posted
Jul 11, 2022

2012 – 2017

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
9
Facility City State ZIP Site status
Prostate Oncology Specialists, Inc. Marina del Rey California 90292 —
IU Health Bloomington Hospital Bloomington Indiana 47403 —
IU Health Goshen Hospital Goshen Indiana 46527 —
Indiana University Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202 —
IU Health Central Indiana Cancer Centers Indianapolis Indiana 46219 —
Northern Indiana Cancer Research Consortium South Bend Indiana 46601 —
Dana Farber Cancer Institute Boston Massachusetts 02115 —
Mayo Clinic Rochester Minnesota 55905 —
University of New Mexico Cancer Center: Albuquerque Albuquerque New Mexico 87131 —
Virginia Oncology Associates Norfolk Virginia 23502 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01681433, 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 Jul 11, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01681433 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →