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Completed Phase 2 Interventional Results available

Bevacizumab and Temsirolimus in Treating Patients With Recurrent or Persistent Endometrial Cancer

ClinicalTrials.gov ID: NCT00723255

Public ClinicalTrials.gov record NCT00723255. 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 11, 2026, 5:32 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 Evaluation of Combination Bevacizumab (NCI-Supplied Agent: NSC #70486) and Temsirolimus (CCI-779, NCI-Supplied Agent, NSC #683864) in the Treatment of Recurrent or Persistent Endometrial Carcinoma

Brief summary

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

This phase II trial is studying the side effects of giving bevacizumab together with temsirolimus and to see how well it works in treating patients with recurrent or persistent endometrial 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. Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for their growth. Giving bevacizumab together with temsirolimus may kill more tumor cells.

Study identification

NCT ID
NCT00723255
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
53 participants

Conditions and interventions

Interventions

Biological · Drug

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
Aug 31, 2008
Primary completion
Jul 14, 2011
Completion
Jan 24, 2016
Last update posted
Jul 22, 2019

2008 – 2016

United States locations

U.S. sites
41
U.S. states
18
U.S. cities
35
Facility City State ZIP Site status
Hartford Hospital Hartford Connecticut 06102
The Hospital of Central Connecticut New Britain Connecticut 06050
Washington Hospital Center Washington D.C. District of Columbia 20010
Memorial University Medical Center Savannah Georgia 31404
Rush University Medical Center Chicago Illinois 60612
University of Chicago Chicago Illinois 60637
Sudarshan K Sharma MD Limted-Gynecologic Oncology Hinsdale Illinois 60521
Elkhart General Hospital Elkhart Indiana 46515
Indiana University Medical Center Indianapolis Indiana 46202
Saint Vincent Hospital and Health Services Indianapolis Indiana 46260
Community Howard Regional Health Kokomo Indiana 46904
IU Health La Porte Hospital La Porte Indiana 46350
Saint Joseph Regional Medical Center-Mishawaka Mishawaka Indiana 46545-1470
Memorial Hospital of South Bend South Bend Indiana 46601
South Bend Clinic South Bend Indiana 46617
Northern Indiana Cancer Research Consortium South Bend Indiana 46628
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
Gynecologic Oncology of West Michigan PLLC Grand Rapids Michigan 49546
Lakeland Hospital Saint Joseph Michigan 49085
University of Mississippi Medical Center Jackson Mississippi 39216
Centerpoint Medical Center LLC Independence Missouri 64057
Truman Medical Center Kansas City Missouri 64108
Mercy Hospital Springfield Springfield Missouri 65804
Ozark Health Ventures LLC-Cancer Research for The Ozarks Springfield Springfield Missouri 65804
Saint Louis University Hospital St Louis Missouri 63110
Washington University School of Medicine St Louis Missouri 63110
Cooper Hospital University Medical Center Camden New Jersey 08103
Women's Cancer Care Associates LLC Albany New York 12208
Memorial Sloan-Kettering Cancer Center New York New York 10065
Carolinas Medical Center Charlotte North Carolina 28203
Gynecologic Oncology Network Greenville North Carolina 27834
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
MetroHealth Medical Center Cleveland Ohio 44109
Riverside Methodist Hospital Columbus Ohio 43214
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Tulsa Cancer Institute Tulsa Oklahoma 74146
Abington Memorial Hospital Abington Pennsylvania 19001
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Women and Infants Hospital Providence Rhode Island 02905
AnMed Health Cancer Center Anderson South Carolina 29621
Carilion Clinic Gynecological Oncology Roanoke Virginia 24016

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 NCT00723255, 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 22, 2019 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00723255 live on ClinicalTrials.gov.

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