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Sponsored by: |
AstraZeneca |
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Information provided by: | AstraZeneca |
ClinicalTrials.gov Identifier: | NCT00681369 |
the purpose of this study is to describe the way Faslodex is used in France, in patients suffering from initial breast cancer, that is to evaluate Faslodex treatment duration and to determine patients profile
Condition |
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Breast Cancer |
Study Type: | Observational |
Study Design: | Cohort, Retrospective |
Official Title: | Observational Usage Study of Faslodex in Patients Suffering From Initial Breast Cancer in France |
Enrollment: | 217 |
Study Start Date: | May 2007 |
Study Completion Date: | June 2007 |
Groups/Cohorts |
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1
Patients suffering from initial breast cancer, treated with Faslodex, treatment which was stopped during 2007
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Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Hospital sample
Inclusion Criteria:
Responsible Party: | AstraZeneca ( Francisco Sapunar - Medical Science Director ) |
Study ID Numbers: | NIS-OFR-FAS-2007/1 |
Study First Received: | May 20, 2008 |
Last Updated: | May 20, 2008 |
ClinicalTrials.gov Identifier: | NCT00681369 |
Health Authority: | France: Haute Autorité de Santé Transparency Commission |
breast cancer fulvestrant longitudinal study France |
Skin Diseases Fulvestrant Breast Neoplasms Breast Diseases |
Neoplasms Neoplasms by Site |