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Terminated Phase 2 Interventional Results available

Temsirolimus in Treating Patients With Recurrent or Persistent Cancer of the Uterus

ClinicalTrials.gov ID: NCT01061606

Public ClinicalTrials.gov record NCT01061606. 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 24, 2026, 2:12 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

Pilot Phase II Study of Temsirolimus in Patients With Recurrent Mixed Mesodermal and Mullerian Tumors (Carcinosarcoma) of the Uterus

Brief summary

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

This phase II trial is studying how well temsirolimus works in treating patients with recurrent or persistent cancer of the uterus. Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Study identification

NCT ID
NCT01061606
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
8 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 31, 2009
Primary completion
Mar 31, 2012
Completion
Sep 30, 2012
Last update posted
Nov 8, 2016

2010 – 2012

United States locations

U.S. sites
20
U.S. states
6
U.S. cities
14
Facility City State ZIP Site status
Tower Cancer Research Foundation Beverly Hills California 90211-1850 —
City of Hope Duarte California 91010 —
Los Angeles County-USC Medical Center Los Angeles California 90033 —
City of Hope Medical Group Inc Pasadena California 91105 —
University of California at Davis Cancer Center Sacramento California 95817 —
University of Connecticut Farmington Connecticut 06030 —
Yale University New Haven Connecticut 06520 —
Morristown Memorial Hospital Morristown New Jersey 07962 —
The Valley Hospital-Luckow Pavilion Paramus New Jersey 07652 —
Women's Cancer Care Associates LLC Albany New York 12208 —
Beth Israel Medical Center New York New York 10003 —
New York University Langone Medical Center New York New York 10016 —
Saint Luke's Roosevelt Hospital Center - Roosevelt Division New York New York 10019 —
Presbyterian-Weill Medical College New York New York 10021 —
Mount Sinai School of Medicine New York New York 10029 —
Children's Hospital of New York Presbyterian New York New York 10032 —
Columbia University College of Physicians and Surgeons New York New York 10032 —
Montefiore Medical Center - Moses Campus The Bronx New York 10467-2490 —
Penn State Hershey Children's Hospital Hershey Pennsylvania 17033 —
University of Texas Health Science Center at San Antonio San Antonio Texas 78229 —

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 NCT01061606, 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 8, 2016 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01061606 live on ClinicalTrials.gov.

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