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Spots Global Cancer Trial Database for Letrozole in Women With Advanced Estrogen/Progesterone Receptor Positive Uterine Leiomyosarcoma

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Letrozole in Women With Advanced Estrogen/Progesterone Receptor Positive Uterine Leiomyosarcoma

Official Title: Phase 2 Clinical Study of Letrozole in Women With Advanced Estrogen/Progesterone Receptor Positive Uterine Leiomyosarcoma

Study ID: NCT00856050

Conditions

Leiomyosarcoma

Interventions

letrozole

Study Description

Brief 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).

Detailed 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

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Contact Details

Name: Suzanne George, MD

Affiliation: Dana-Farber Cancer Institute

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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