Faslodex Observations During Regular Use by Advanced Mammacarcinoma Patients
NCT00241462 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 150
Last updated 2009-04-22
Summary
The purpose of this study is to identify which patients, receiving Faslodex within the approved label, benefit most from Faslodex treatment.
Conditions
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
AstraZeneca Netherlands Medical Director, MD · AstraZeneca
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-06-30
- Completion
- 2009-12-31
Countries
- Netherlands
Study Locations
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