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Spots Global Cancer Trial Database for Faslodex Post Marketing Surveillance

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Faslodex Post Marketing Surveillance

Official Title: Faslodex Post Marketing Surveillance

Study ID: NCT00860561

Conditions

Breast Cancer

Interventions

Study Description

Brief Summary: 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 any unknown adverse events of Faslodex.

Detailed Description:

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Research Site, Cheonan, , Korea, Republic of

Research Site, Daegu, , Korea, Republic of

Research Site, Daejeon, , Korea, Republic of

Research Site, Iksan, , Korea, Republic of

Research Site, Jeonju, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Suwon-si, , Korea, Republic of

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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