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Completed Phase 1Phase 2 Interventional

Safety and Tolerability Study of ISIS EIF4E Rx in Combination With Docetaxel and Prednisone (CRPC)

ClinicalTrials.gov ID: NCT01234025

Public ClinicalTrials.gov record NCT01234025. 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 26, 2026, 6:09 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 Phase 1b/2 Study of Docetaxel and Prednisone, With or Without ISIS 183750 (an eIF4E Inhibitor), in Patients With Castrate-Resistant Prostate Cancer

Brief summary

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

The purpose of this study is to examine the safety, tolerability and progression-free survival of patients with Castrate-Resistant Prostate Cancer treated with ISIS EIF4E Rx in combination with docetaxel and prednisone.

Study identification

NCT ID
NCT01234025
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Ionis Pharmaceuticals, Inc.
Industry
Enrollment
113 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
Nov 2010 (Type not available)
Primary completion
May 2013 (Actual)
Completion
Dec 2013 (Actual)
Last update posted
Oct 6, 2023

2010 – 2013

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Highlands Oncology Group Fayetteville Arkansas 72703 —
San Bernardino Urological Associates San Bernardino California 92404-4816 —
Fort Range Cancer Center Fort Collins Colorado 80528 —
Norwalk Hospital- Whittingham Cancer Center Norwalk Connecticut 06850 —
Lakeland Regional Cancer Center Lakeland Florida 33805 —
University of Miami, Miller School of Medicine - Sylvester Comprehensive Cancer Center Miami Florida 33136 —
Central Baptist Hospital Clinical Research Center Lexington Kentucky 40503 —
Feist-Weiller Cancer Center, Louisiana State University Health Sciences Center Shreveport Louisiana 71103 —
St. Luke's - Roosevelt Hospital Center New York New York 10019 —
James P. Wilmont Cancer Center - University of Rochester Medical Center Rochester New York 14642 —
Gabrail Cancer Center Canton Ohio 44718 —

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 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01234025, 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 6, 2023 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01234025 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →