Faslodex Observations During Regular Use by Advanced Mammacarcinoma Patients

NCT00241462 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2009-04-22

No results posted yet for this study

Summary

The purpose of this study is to identify which patients, receiving Faslodex within the approved label, benefit most from Faslodex treatment.

Conditions

Sponsors & Collaborators

Principal Investigators

  • AstraZeneca Netherlands Medical Director, MD · AstraZeneca

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-06-30
Completion
2009-12-31

Countries

  • Netherlands

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 NCT00241462 on ClinicalTrials.gov