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Completed Phase 2 Interventional

Study to Evaluate the Efficacy, Safety, and Tolerability of E7070 in Metastatic Breast Cancer Patients

ClinicalTrials.gov ID: NCT00080197

Public ClinicalTrials.gov record NCT00080197. 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 Apr 29, 2026, 5:05 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

An Open-Label Phase II Study of E7070 in Metastatic Breast Cancer Patients Previously Treated With an Anthracycline, a Taxane, and Capecitabine

Study identification

NCT ID
NCT00080197
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
250 participants

Conditions and interventions

Interventions

  • E7070 Drug

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
Jan 31, 2004
Primary completion
Not listed
Completion
Apr 30, 2005
Last update posted
Oct 10, 2006

2004 – 2005

United States locations

U.S. sites
34
U.S. states
19
U.S. cities
34
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Hoover Alabama
Not listed Sedona Arizona
Not listed Denver Colorado
Not listed Torrington Connecticut
Not listed Fort Myers Florida
Not listed Ocoee Florida
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Skokie Illinois
Not listed Urbana Illinois
Not listed Indianapolis Indiana
Not listed Overland Park Kansas
Not listed Minneapolis Minnesota
Not listed St Louis Missouri
Not listed Albany New York
Not listed Winston-Salem North Carolina
Not listed Kettering Ohio
Not listed Oklahoma City Oklahoma
Not listed Tulsa Oklahoma
Not listed Clairton Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Wexford Pennsylvania
Not listed Greenville South Carolina
Not listed Austin Texas
Not listed Dallas Texas
Not listed Fort Worth Texas
Not listed Fredericksburg Texas
Not listed Houston Texas
Not listed Irving Texas
Not listed Tyler Texas
Not listed Fairfax Virginia
Not listed Spokane Washington
Not listed Vancouver 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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00080197, 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 10, 2006 · Synced Apr 29, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00080197 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →