Trial Information

Summary: A Phase II Evaluation of Docetaxel and Gemcitabine + G-CSF in the Treatment of Recurrent or Persistent Leimyosarcoma of the Uterus

This research study is for women who have been diagnosed with uterine cancer, specifically leiomyosarcoma, that has come back or continues to grow after initial standard surgery and chemotherapy. The purpose of this study is to compare the effectiveness and safety of treating cancer of the uterus using a combination of two chemotherapy drugs: docetaxel and gemcitabine. Study participants will receive both docetaxel and gemcitabine.
No Compensation Provided

Patient Inclusion/Exclusion Criteria:

You may be eligible to participate if you
-are 18 years of age or older
-have recurrent or persistent leiomyosarcoma of the uterus which is resistant to surgery and chemotherapy
-meet additional criteria

You cannot participate in this study if you
-are pregnant or breastfeeding
-have had prior therapy with docetaxel or gemcitabine

Contact:

Rudy Segna, MD, Prinicpal Investigator
Mount Sinai Medical Center
One Gustave L. Levy Place

New York, NY 10029
Telephone: 212-888-8439
Fax: 212-319-1140
Email:

If you would like to learn more about participating in this study, please send an e-mail message using the form below.

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Trial listings updated: June 1, 2008 at 5:45:36 AM


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