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Clinical Trial Summary

The purpose of this research study is to determine if letrozole is effective at controlling the growth or spread of estrogen and/or progesterone receptor positive uterine leiomyosarcoma. This drug has been used in research studies for other cancers and is currently approved by the FDA for use in breast cancer. Because letrozole lowers hormone levels in the body, it may be helpful to control tumors that express hormone receptors ( ER/PR).


Clinical Trial Description

- Participants will take letrozole orally once a day. During the research study the following tests and procedures will be performed:

- Visit 1 (Day 1): physical examination, vital signs and blood work

- Visit 2 (Day 43): physical examination, vital signs, blood work, CT or MRI scan

- Visit 3 (Day 85): physical examination, vital signs, blood work, CT or MRI scan

- Participants will remain on the study drug as long as they do not have any serious sife effect and their disease does not get worse ;


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00856050
Study type Interventional
Source Dana-Farber Cancer Institute
Contact
Status Completed
Phase Phase 2
Start date February 2009
Completion date March 2014

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