Faslodex Specific Clinical Experience Investigation
NCT01501266 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 660
Last updated 2016-05-10
Summary
The purpose of this study is to confirm the safety profile such as the frequency of serious adverse events or any unexpected adverse events and overall efficacy of Faslodex for long term treatment in daily clinical practice.
Conditions
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Shigeru Yoshida · AstraZeneca KK
Eligibility
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-02-29
- Primary Completion
- 2015-01-31
- Completion
- 2015-01-31
Countries
- Japan
Study Locations
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