Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Sep 4, 2026, 2:48 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

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
Jul 31, 2006
Primary completion
Feb 28, 2007
Completion
Jan 31, 2008
Last update posted
Nov 24, 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 24, 2019 · Synced Sep 4, 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 NCT00394251 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →