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Terminated Phase 3 Interventional

Comparison of Safety and Efficacy of TOCOSOL(R) Paclitaxel Versus Taxol(R) for Treatment of Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00251095

Public ClinicalTrials.gov record NCT00251095. 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 Nov 7, 2026, 9:21 AM EST

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Official title

A Multicenter Phase 3, Randomized Comparison of the Safety and Efficacy of Weekly TOCOSOL(R) Paclitaxel vs. Weekly Paclitaxel Injection in the Treatment of Metastatic Breast Cancer

Brief summary

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

The purpose of this study is to compare the objective response rates of patients randomized to receive either TOCOSOL(R) Paclitaxel or Taxol(R) (paclitaxel injection) administered every week to patients with metastatic breast cancer. The study hypothesis is that the objective response rate with TOCOSOL Paclitaxel given every week is non-inferior to that observed with Taxol given every week.

Study identification

NCT ID
NCT00251095
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Achieve Life Sciences
Industry
Enrollment
821 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
Sep 2005 (Type not available)
Primary completion
Sep 2007 (Actual)
Completion
Sep 2007 (Actual)
Last update posted
Jun 4, 2009

2005 – 2007

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Alta Bates Comprehensive Cancer Center Berkeley California 94704 —
Desert Hematology Oncology Medical Group Rancho Mirage California 92270 —
Stockton Hematology Oncology Stockton California 95204 —
Florida Cancer Specialists Fort Myers Florida 33901 —
Mountain State Tumor Institute Boise Idaho 83712 —
Oncology Care Associates Saint Joseph Michigan 49085 —
Southfield Oncology Institute, Inc Southfield Michigan 48076 —
Norris Cotton Cancer Center, Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
Essex Oncology of North Jersey Belleville New Jersey 07109 —
Mid Dakota Clinic Bismarck North Dakota 58501 —
Hematology Oncology Consultants, Inc Columbus Ohio 43235 —
Chattanooga Oncology & Hematology Associates, PC Chattanooga Tennessee 37404 —
The Sarah Cannon Research Institute Nashville Tennessee 37203 —
Joe Arrington Cancer Research and Treatment Center Lubbock Texas 79410 —

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 NCT00251095, 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 Jun 4, 2009 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00251095 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →