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Completed Phase 2 Interventional Results available

Bevacizumab With or Without Fosbretabulin Tromethamine in Treating Patients With Recurrent or Persistent Ovarian Epithelial, Fallopian Tube, or Peritoneal Cavity Cancer

ClinicalTrials.gov ID: NCT01305213

Public ClinicalTrials.gov record NCT01305213. 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 23, 2026, 5:30 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

A Randomized Phase II Evaluation of Single-Agent Bevacizumab (NSC #704865) and Combination Bevacizumab With Fosbretabulin Tromethamine (CA4P) (NSC #752293) in the Treatment of Recurrent or Persistent Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Carcinoma

Brief summary

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

This randomized phase II trial studies how well bevacizumab with or without fosbretabulin tromethamine works in treating patients with ovarian epithelial, fallopian tube, or peritoneal cavity cancer that has come back or is persistent. Monoclonal antibodies, such as bevacizumab, find tumor cells and help kill them. Bevacizumab and fosbretabulin tromethamine may stop the growth of ovarian cancer by blocking blood flow to the tumor. It is not yet known whether bevacizumab is more effective with or without fosbretabulin tromethamine in treating ovarian epithelial, fallopian tube, and peritoneal cavity cancer.

Study identification

NCT ID
NCT01305213
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
107 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
Mar 21, 2011 (Actual)
Primary completion
Aug 20, 2016 (Actual)
Completion
Nov 3, 2016 (Actual)
Last update posted
Jul 30, 2019

2011 – 2016

United States locations

U.S. sites
51
U.S. states
27
U.S. cities
43
Facility City State ZIP Site status
Saint Joseph's Hospital and Medical Center Phoenix Arizona 85013 —
Providence Saint Joseph Medical Center/Disney Family Cancer Center Burbank California 91505 —
John Muir Medical Center-Concord Campus Concord California 94520 —
UC San Diego Moores Cancer Center La Jolla California 92093 —
Cedars Sinai Medical Center Los Angeles California 90048 —
Sutter Medical Center Sacramento Sacramento California 95816 —
Penrose-Saint Francis Healthcare Colorado Springs Colorado 80907 —
Presbyterian - Saint Lukes Medical Center - Health One Denver Colorado 80218 —
SCL Health Lutheran Medical Center Wheat Ridge Colorado 80033 —
Hartford Hospital Hartford Connecticut 06102 —
Beebe Medical Center Lewes Delaware 19958 —
Christiana Care Health System-Christiana Hospital Newark Delaware 19718 —
Mercy Hospital Miami Florida 33133 —
Northeast Georgia Medical Center-Gainesville Gainesville Georgia 30501 —
Memorial Health University Medical Center Savannah Georgia 31404 —
Saint Alphonsus Cancer Care Center-Boise Boise Idaho 83706 —
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637 —
Sudarshan K Sharma MD Limited-Gynecologic Oncology Hinsdale Illinois 60521 —
Indiana University/Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202 —
Saint Vincent Hospital and Health Care Center Indianapolis Indiana 46260 —
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242 —
Maine Medical Center-Bramhall Campus Portland Maine 04102 —
Sinai Hospital of Baltimore Baltimore Maryland 21215 —
MedStar Franklin Square Medical Center/Weinberg Cancer Institute Baltimore Maryland 21237 —
University of Massachusetts Memorial Health Care Worcester Massachusetts 01605 —
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109 —
Bronson Methodist Hospital Kalamazoo Michigan 49007 —
West Michigan Cancer Center Kalamazoo Michigan 49007 —
Borgess Medical Center Kalamazoo Michigan 49048 —
Saint Dominic-Jackson Memorial Hospital Jackson Mississippi 39216 —
University of Mississippi Medical Center Jackson Mississippi 39216 —
Washington University School of Medicine St Louis Missouri 63110 —
Women's Cancer Center of Nevada Las Vegas Nevada 89169 —
Novant Health Presbyterian Medical Center Charlotte North Carolina 28204 —
Duke University Medical Center Durham North Carolina 27710 —
Summa Akron City Hospital/Cooper Cancer Center Akron Ohio 44304 —
University of Cincinnati/Barrett Cancer Center Cincinnati Ohio 45219 —
Cleveland Clinic Cancer Center/Fairview Hospital Cleveland Ohio 44111 —
Hillcrest Hospital Cancer Center Mayfield Heights Ohio 44124 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
Women and Infants Hospital Providence Rhode Island 02905 —
Greenville Health System Cancer Institute-Eastside Greenville South Carolina 29615 —
Sanford Cancer Center Oncology Clinic Sioux Falls South Dakota 57104 —
Sanford USD Medical Center - Sioux Falls Sioux Falls South Dakota 57117-5134 —
Virginia Commonwealth University/Massey Cancer Center Richmond Virginia 23298 —
Green Bay Oncology at Saint Vincent Hospital Green Bay Wisconsin 54301-3526 —
Saint Vincent Hospital Cancer Center Green Bay Green Bay Wisconsin 54301 —
Green Bay Oncology Limited at Saint Mary's Hospital Green Bay Wisconsin 54303 —
Holy Family Memorial Hospital Manitowoc Wisconsin 54221 —
Bay Area Medical Center Marinette Wisconsin 54143 —

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 NCT01305213, 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 Jul 30, 2019 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01305213 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →