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Completed Phase 2 Interventional Results available

Bevacizumab With or Without Everolimus in Treating Patients With Recurrent or Persistent Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer

ClinicalTrials.gov ID: NCT00886691

Public ClinicalTrials.gov record NCT00886691. 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 26, 2026, 3:04 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 Phase II Randomized, Double-Blinded Evaluation of Oral Everolimus (RAD001) Plus Bevacizumab vs. Oral Placebo Plus Bevacizumab in the Treatment of Recurrent or Persistent Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer

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 everolimus works in treating patients with recurrent or persistent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab and everolimus may also stop the growth of tumor cells by blocking blood flow to the tumor. It is not yet known whether bevacizumab is more effective when given together with or without everolimus in treating ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer.

Study identification

NCT ID
NCT00886691
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GOG Foundation
Network
Enrollment
150 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
Dec 27, 2010 (Actual)
Primary completion
Jun 27, 2014 (Actual)
Completion
Mar 23, 2015 (Actual)
Last update posted
Feb 4, 2022

2010 – 2015

United States locations

U.S. sites
45
U.S. states
22
U.S. cities
35
Facility City State ZIP Site status
Gynecologic Oncology Group of Arizona Phoenix Arizona 85012 —
Providence Saint Joseph Medical Center/Disney Family Cancer Center Burbank California 91505 —
Cedars Sinai Medical Center Los Angeles California 90048 —
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California 92868 —
University of Colorado Hospital Aurora Colorado 80045 —
The Hospital of Central Connecticut New Britain Connecticut 06050 —
Rush University Medical Center Chicago Illinois 60612 —
Sudarshan K Sharma MD Limited-Gynecologic Oncology Hinsdale Illinois 60521 —
Carle Cancer Center Urbana Illinois 61801 —
Indiana University/Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202 —
Saint Vincent Hospital and Health Care Center Indianapolis Indiana 46260 —
McFarland Clinic PC - Ames Ames Iowa 50010 —
Iowa Methodist Medical Center Des Moines Iowa 50309 —
Iowa-Wide Oncology Research Coalition NCORP Des Moines Iowa 50309 —
Medical Oncology and Hematology Associates-Des Moines Des Moines Iowa 50309 —
Medical Oncology and Hematology Associates-Laurel Des Moines Iowa 50314 —
Mercy Medical Center - Des Moines Des Moines Iowa 50314 —
Iowa Lutheran Hospital Des Moines Iowa 50316 —
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242 —
Baystate Medical Center Springfield Massachusetts 01199 —
Saint Joseph Mercy Hospital Ann Arbor Michigan 48106 —
Mercy Hospital Springfield Springfield Missouri 65804 —
CoxHealth South Hospital Springfield Missouri 65807 —
Nebraska Methodist Hospital Omaha Nebraska 68114 —
Cooper Hospital University Medical Center Camden New Jersey 08103 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Carolinas Medical Center/Levine Cancer Institute Charlotte North Carolina 28203 —
Duke University Medical Center Durham North Carolina 27710 —
Case Western Reserve University Cleveland Ohio 44106 —
MetroHealth Medical Center Cleveland Ohio 44109 —
Cleveland Clinic Cancer Center/Fairview Hospital Cleveland Ohio 44111 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
Riverside Methodist Hospital Columbus Ohio 43214 —
Hillcrest Hospital Cancer Center Mayfield Heights Ohio 44124 —
UH Seidman Cancer Center at Lake Health Mentor Campus Mentor Ohio 44060 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Oklahoma Cancer Specialists and Research Institute-Tulsa Tulsa Oklahoma 74146 —
Jefferson Abington Hospital Abington Pennsylvania 19001 —
University of Pennsylvania/Abramson Cancer Center Philadelphia Pennsylvania 19104 —
Reading Hospital West Reading Pennsylvania 19611 —
Women and Infants Hospital Providence Rhode Island 02905 —
AnMed Health Cancer Center Anderson South Carolina 29621 —
Baylor All Saints Medical Center at Fort Worth Fort Worth Texas 76104 —
LDS Hospital Salt Lake City Utah 84143 —
University of Wisconsin Hospital and Clinics Madison Wisconsin 53792 —

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 NCT00886691, 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 Feb 4, 2022 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00886691 live on ClinicalTrials.gov.

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