Expired Study
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Dallas, Texas 75204


Purpose:

This is an open-label, multicenter, randomized (1:1 randomization ratio) study of either exemestane or exemestane plus celecoxib in postmenopausal women with ABC having progressed on tamoxifen.


Criteria:

Inclusion Criteria: - Postmenopausal female patient with histologically or cytologically confirmed breast cancer having progressed on Tamoxifen. - Advanced disease: patients with advanced breast carcinoma with disease progression who had progressed/relapsed following > 8 weeks of treatment with Tamoxifen for advanced disease; or progressed during adjuvant Tamoxifen for at least 6 or 12 months depending on receptor status; or progressed within 12 months from completion of adjuvant treatment with Tamoxifen. - at least one measurable lesion Exclusion Criteria: - More than one previous chemotherapy and/or more than one hormonotherapy for advanced disease. - Previous hormonotherapy for advanced disease other than Tamoxifen. - Myocardial infarction within previous 6 mo


NCT ID:

NCT00038103


Primary Contact:

Study Director
Pfizer CT.gov Call Center
Pfizer


Backup Contact:

N/A


Location Contact:

Dallas, Texas 75204
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 14, 2017

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