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Completed Phase 3 Interventional Results available

E7389 Versus Treatment of Physician's Choice in Patients With Locally Recurrent or Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00388726

Public ClinicalTrials.gov record NCT00388726. 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 Sep 25, 2026, 1:31 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

The "EMBRACE" Trial: Eisai Metastatic Breast Cancer Study Assessing Physician's Choice Versus E7389. A Phase III Open-Label, Randomized, Parallel, Two-arm, Multi-center Study of E7389 Versus "Treatment of Physician's Choice" in Patients With Locally Recurrent, Metastatic Breast Cancer, Previously Treated With At Least Two and a Maximum of Five Prior Chemotherapy Regimens, Including an Anthracycline and a Taxane

Brief summary

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

The purpose of this study is to compare Overall Survival (OS), Progression Free Survival (PFS), objective tumor response rate, duration of response, and safety in patients treated with E7389 versus the Treatment of Physician's Choice (TPC) in patients with locally recurrent or metastatic breast cancer.

Study identification

NCT ID
NCT00388726
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eisai Inc.
Industry
Enrollment
762 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Oct 31, 2006
Primary completion
Apr 30, 2009
Completion
May 31, 2013
Last update posted
Jan 6, 2020

2006 – 2013

United States locations

U.S. sites
32
U.S. states
18
U.S. cities
32
Facility City State ZIP Site status
US Oncology St. Vincent's Hospital - Bruno Cancer Center Birmingham Alabama — —
Bellflower Satellite Bellflower California — —
Research Center Gilroy California 95020 —
US Oncology Denver Colorado — —
Florida Cancer Research Institute Davie Florida — —
Innovative Medical Research of South Florida, Inc. Miami Florida 33179 —
Peachtree Hematology/Oncology Consultants, PC Atlanta Georgia — —
US Oncology Niles Illinois — —
US Oncology Indianapolis Indiana — —
University of Iowa Hospital and Clinic Iowa City Iowa — —
Hematology Oncology Clinic Baton Rouge Louisiana — —
Oncology Care Associates, P.L.L.C. Saint Joseph Michigan — —
US Oncology Columbia Missouri — —
Montana Cancer Specialists Missoula Montana 59820 —
US Oncology Las Vegas Nevada — —
US Oncology Albany New York — —
North Shore Hematology/Oncology Associates East Setauket New York — —
Weill Cornell Breast Cancer Center New York New York — —
Carolina Hematology Oncology Associates Charlotte North Carolina — —
US Oncology Raleigh North Carolina — —
US Oncology Eugene Oregon — —
St. Vincent Medical Center Portland Oregon — —
US Oncology Bedford Texas — —
US Oncology Dallas Texas — —
US Oncology Houston Texas — —
US Oncology McAllen Texas — —
US Oncology Midland Texas — —
US Oncology Tyler Texas — —
US Oncology Spokane Washington — —
Northwest Medical Specialists Tacoma Washington 98401 —
US Oncology Vancouver Washington — —
US Oncology Yakima Washington — —

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 105 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00388726, 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 Jan 6, 2020 · Synced Sep 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00388726 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →