Faslodex Specific Clinical Experience Investigation

NCT01501266 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 660

Last updated 2016-05-10

No results posted yet for this study

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

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01501266 on ClinicalTrials.gov