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Faslodex Post Marketing Surveillance | Clinical Trials | Clareo Health

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COMPLETEDNCT00860561

Faslodex Post Marketing Surveillance

This PMS aims to assess the efficacy, the safety and tolerability profile of Faslodex in everyday practice. Secondary objective of this PMS is to identify the frequency of serious adverse events or an...

Lead sponsor: AstraZeneca•7 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

AstraZeneca

Age

All ages

Sex

FEMALE

Healthy Volunteers

No

Inclusion Criteria

•Postmenopausal women
•Patients who have failed 2 or more prior hormone therapies (The prior hormone therapies should contain both antiestrogen and non-steroidal Aromatase inhibitor)
•Patients who were intolerant to prior hormone therapy and have no endocrine therapeutic options (The prior hormone therapies should contain both antiestrogen and non-steroidal Aromatase inhibitor)

Exclusion Criteria

•The patients who received Faslodex treatment before

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: October 10, 2014Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment42

Start dateJan 2009

Last updatedOct 10, 2014

Condition

Locations shown

Research Site

Cheonan

Research Site

Daegu

Research Site

Daejeon

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 10, 2014Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions