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Completed Phase 2 Interventional

Evaluation of a New Agent for Treatment of Advanced Stage Breast Cancer

ClinicalTrials.gov ID: NCT00313248

Public ClinicalTrials.gov record NCT00313248. 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 2, 2026, 3:54 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

Phase 2 Study to Investigate the Efficacy and Safety of ZK-Epothilone (ZK-Epo; ZK 219477) in Patients With Metastatic Breast Cancer

Brief summary

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

The purpose of this study is to evaluate whether treatment with a new drug called ZK-Epothilone (ZK-Epo) in patients with metastatic breast cancer helps to decrease or stop tumor growth.

Study identification

NCT ID
NCT00313248
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bayer
Industry
Enrollment
65 participants

Conditions and interventions

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
Mar 31, 2006
Primary completion
Sep 30, 2008
Completion
Oct 31, 2008
Last update posted
Dec 9, 2015

2006 – 2008

United States locations

U.S. sites
21
U.S. states
18
U.S. cities
21
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233
Not listed Anchorage Alaska 99508
Not listed Tucson Arizona 85724
Not listed Hot Springs Arkansas 71913
Not listed Bakersfield California 93309
Not listed Palm Springs California 92262
Not listed Aurora Colorado 80010
Not listed Washington D.C. District of Columbia 20007
Not listed Daytona Beach Florida 32114
Not listed Decatur Illinois 62526
Not listed New Albany Indiana 47150
Not listed Baltimore Maryland 21204
Not listed Minneapolis Minnesota 55455
Not listed Livingston New Jersey 07039
Not listed New York New York 10021
Not listed Syracuse New York 13210
Not listed Portland Oregon 97239
Not listed Pittsburgh Pennsylvania 15213-3180
Not listed Houston Texas 77030
Not listed San Antonio Texas 78207
Not listed Tacoma Washington 98405

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00313248, 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 Dec 9, 2015 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00313248 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →