Status:

COMPLETED

Faslodex Specific Clinical Experience Investigation

Lead Sponsor:

AstraZeneca

Conditions:

Breast Cancer

Eligibility:

FEMALE

Brief 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 ...

Detailed Description

MC MD

Eligibility Criteria

Inclusion

  • Patients treated with Faslodex for the first time due to postmenopausal breast cancer

Exclusion

  • None

Key Trial Info

Start Date :

February 1 2012

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

January 1 2015

Estimated Enrollment :

660 Patients enrolled

Trial Details

Trial ID

NCT01501266

Start Date

February 1 2012

End Date

January 1 2015

Last Update

May 10 2016

Active Locations (43)

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Page 1 of 11 (43 locations)

1

Research Site

Aichi, Japan

2

Research Site

Akita, Japan

3

Research Site

Aomori, Japan

4

Research Site

Chiba, Japan