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Randomized Phase II Trial of Letrozole With or Without Dasatinib as First and Second-line Treatment for Hormone Receptor-positive, HER2-negative Post-menopausal Breast Cancer That is Unresectable, Locally Recurrent or Metastatic

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City:   Yakima
State:   Washington
Zip Code:   98902
Conditions:   Metastatic Breast Cancer
Purpose:   The purpose of this study is to find out what effect the combination of letrozole (brand name: Femara) and dasatinib (brand name: Sprycel) has on metastatic breast cancer compared to letrozole alone
Study Summary:  
Criteria:   Inclusion Criteria: - Has histologic or cytologic diagnosis of breast cancer; evidence of unresectable locally recurrent or metastatic disease - Has measurable or evaluable-only disease - Is female, ≥18 yrs of age, post menopausal or surgically sterile - HER2 negative, HR+, ER+ and/or PgR+ breast cancer - 0-1 prior chemotherapy regimen for metastatic disease. - Prior adjuvant or neoadjuvant chemotherapy completed at least 1 month prior - Prior tamoxifen therapy is allowed - No AI therapy for >1 year without recurrence Exclusion Criteria: - Pregnant or breast feeding - Prior hormonal therapy for metastatic or locally recurrent disease - >1 chemotherapy regimen for metastatic disease - Pleural or pericardial effusion - Serious cardiac condition
NCT ID:   NCT00696072
Primary Contact:   Study Director
Bristol-Myers Squibb
Bristol-Myers Squibb

For participation information at a USA site use a phone number below. For site information outside the USA please email:
Email: Clinical.Trials@bms.com
Backup Contact:   First line of email MUST contain NCT# & Site#. Only trial sites that are recruiting have contact information at this time.
Location Contact:   Yakima, Washington 98902
United States

Vicky E. Jones, Site 023

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 25, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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