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Completed Phase 2 Interventional Results available

Bevacizumab With Abraxane in Patients With Recurrent Ovarian/ Peritoneal Cancer

ClinicalTrials.gov ID: NCT00407563

Public ClinicalTrials.gov record NCT00407563. 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 17, 2026, 2:00 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

A Phase 2 Study of Bevacizumab With Abraxane in Patients With Recurrent, Platinum-Resistant Primary Epithelial Ovarian or Primary Peritoneal Carcinoma

Brief summary

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

The purpose of this study is to evaluate the effectiveness and tolerability of the combination of bevacizumab and Abraxane in the treatment of women with epithelial ovarian cancer or peritoneal cancer. The study will also evaluate how the patient's quality of life is during their treatment.

Study identification

NCT ID
NCT00407563
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
48 participants

Conditions and interventions

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
Jan 2007 (Type not available)
Primary completion
Feb 2011 (Actual)
Completion
Feb 2011 (Actual)
Last update posted
Apr 5, 2012

2007 – 2011

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Little Rock Hematology Oncology Little Rock Arkansas 72205 —
Wilshire Oncology Medical Group, Inc. La Verne California 91750 —
Northeast Georgia Cancer Care, LLC Athens Georgia 30607 —
Southeastern Gynecologic Oncology, LLC Atlanta Georgia 30342 —
North Idaho Cancer Center Coeur d'Alene Idaho 38314 —
Hematology-Oncology Centers of the Northern Rockies Billings Montana 59101 —
Mid-Ohio Oncology/Hematology Columbus Ohio 43219 —
Pennsylvania Oncology Hematology Assoc. Philadelphia Pennsylvania 19106 —
Chattanooga's Program in Women's Oncology Chattanooga Tennessee 37403 —
The West Clinic Memphis Tennessee 38120 —
Cancer Specialists of Tidewater, Ltd Chesapeake Virginia 23320 —

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 NCT00407563, 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 5, 2012 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00407563 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →