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Completed Phase 2 Interventional

ZK-Epo Given With Prednisone in Patients With Metastatic Androgen-independent Prostate Cancer

ClinicalTrials.gov ID: NCT00350051

Public ClinicalTrials.gov record NCT00350051. 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, 9:24 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 of ZK-Epothilone (ZK-Epo; ZK219477) Plus Prednisone as First-line Chemotherapy in Patients With Metastatic Androgen-independent Prostate Cancer

Study identification

NCT ID
NCT00350051
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bayer
Industry
Enrollment
53 participants

Conditions and interventions

Interventions

  • Sagopilone (ZK 219477) + prednisone Drug

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
Jul 31, 2006
Primary completion
Sep 23, 2008
Completion
Dec 20, 2009
Last update posted
Apr 7, 2021

2006 – 2009

United States locations

U.S. sites
12
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
Not listed Fountain Valley California 92708
Not listed Sarasota Florida 34237
Not listed Baltimore Maryland 21201
Not listed Ann Arbor Michigan 48109
Not listed Billings Montana 59101
Not listed Omaha Nebraska 68198-7680
Not listed The Bronx New York 10469
Not listed Canton Ohio 44718
Not listed Portland Oregon 97201
Not listed Altoona Pennsylvania 16601
Not listed Fort Worth Texas 76104
Not listed Seattle Washington 98108-1597

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00350051, 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 Apr 7, 2021 · 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 NCT00350051 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →