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Completed Phase 2 Interventional Results available

Evaluating E7389 in Patients With Hormone Refractory Prostate Cancer With Advanced and/or Metastatic Disease Stratified by Prior Chemotherapy

ClinicalTrials.gov ID: NCT00278993

Public ClinicalTrials.gov record NCT00278993. 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 24, 2026, 12:26 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 II, Multicenter, Open Label, Two Stage Design Study Evaluating E7389 in Patients With Hormone Refractory Prostate Cancer With Advanced and/or Metastatic Disease Stratified by Prior Chemotherapy

Brief summary

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

This is a multi-centre, phase II, open-label, two-stage design, single-arm study in patients with hormone-refractory prostate cancer (HRPC) with advanced (rising PSA) and/or metastatic disease and who have had prior anti-androgen therapy. The study will further explore the efficacy of E7389 by enrollment of patients into two strata: those who have had no prior systemic chemotherapy for their disease (except for mitoxantrone and estramustine), and those who failed no more than one previous chemotherapeutic regimen with tubulin-binding agents such as docetaxel.

Study identification

NCT ID
NCT00278993
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
108 participants

Conditions and interventions

Interventions

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
Jan 2006 (Type not available)
Primary completion
Jan 2008 (Actual)
Completion
Jan 2008 (Actual)
Last update posted
Jul 14, 2014

2006 – 2008

United States locations

U.S. sites
18
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Dr. Robert Jotte Denver Colorado 80218 —
Melbourne Internal Medicine Associates Melbourne Florida 32901 —
Ocala Oncology Center PL Ocala Florida 34474 —
Central Indiana Cancer Centers Indianapolis Indiana 46227 —
Minnesota Hematology Oncology Burnsville Minnesota 33557 —
Missouri Cancer Associates Columbia Missouri 65201 —
New York Oncology Hematology, P.C. Albany New York 12208 —
St. Luke's Roosevelt Hospital Center New York New York 10019 —
Columbia University Medical Center New York New York 10032 —
Raleigh Hematology Oncology Associates PL Raleigh North Carolina 27607 —
US Oncology Dallas Texas 75204 —
Mary Crowley Medical Research Center Dallas Texas 75246 —
El Paso Cancer Treatment Center El Paso Texas 79915 —
Texas Oncology PA Fort Worth Texas 76104 —
Texas Oncology PA Tyler Texas 75702 —
Tyler Cancer Center Tyler Texas 75702 —
Deke Slayton Cancer Center Webster Texas 77598 —
Virginia Oncology Associates Norfolk Virginia 23505 —

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 NCT00278993, 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 14, 2014 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00278993 live on ClinicalTrials.gov.

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