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Completed Phase 2 Interventional Results available

Study of Dose-dense Adriamycin Plus Cytoxan (AC) Followed by Either ABI-007 (Abraxane) or Taxol With Bevacizumab as Adjuvant Therapy for Patients With Breast Cancer

ClinicalTrials.gov ID: NCT00394251

Public ClinicalTrials.gov record NCT00394251. 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 Oct 20, 2026, 2:45 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, Randomized, Comparative Pilot Study of Dose-dense Adriamycin Plus Cytoxan (AC) Followed by Either ABI-007 (Abraxane) or Taxol With Bevacizumab as Adjuvant Therapy for Patients With Breast Cancer

Brief summary

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

The primary objective of this study was to compare the safety of dose-dense ABI-007 (Abraxane) 260 mg/m\^2 or Taxol 175 mg/m\^2 given every 2 weeks following dose-dense Adriamycin plus Cytoxan (AC) chemotherapy. Bevacizumab was administered at 10 mg/kg every 2 weeks throughout chemotherapy, and then at 15 mg/kg every 3 weeks following chemotherapy.

Study identification

NCT ID
NCT00394251
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
197 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Aug 1, 2006 (Actual)
Primary completion
Mar 1, 2007 (Actual)
Completion
Feb 1, 2008 (Actual)
Last update posted
Nov 25, 2019

2006 – 2008

United States locations

U.S. sites
27
U.S. states
14
U.S. cities
26
Facility City State ZIP Site status
Not listed Birmingham Alabama 35205 —
Not listed Sedona Arizona 86336 —
Not listed Denver Colorado 80220 —
Not listed Torrington Connecticut 06790 —
Not listed Indianapolis Indiana 46227 —
Not listed Minneapolis Minnesota 55404 —
Not listed Columbia Missouri 65201 —
Not listed St Louis Missouri 63136 —
Not listed Henderson Nevada 89052 —
Not listed Raleigh North Carolina 27607 —
Not listed Eugene Oregon 97401 —
Not listed Greenville South Carolina 29615 —
Not listed Austin Texas 78731 —
Not listed Bedford Texas 76022 —
Not listed Dallas Texas 75231 —
Not listed Dallas Texas 75246 —
Not listed El Paso Texas 79915 —
Not listed Fort Worth Texas 76104 —
Not listed Fredericksburg Texas 78624 —
Not listed Houston Texas 77024 —
Not listed Longview Texas 75601 —
Not listed McAllen Texas 78503 —
Not listed Tyler Texas 75702 —
Not listed Waco Texas 76712 —
Not listed Fairfax Virginia 22031 —
Not listed Norfolk Virginia 23502 —
Not listed Vancouver Washington 98684 —

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 NCT00394251, 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 Nov 25, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00394251 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →