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Clinical Trials/JPRN-UMIN000011976
JPRN-UMIN000011976Completed未知

Observation study to examine the efficacy of 500mg Fluvestrant that targets ER(+) postmenopausal metastatic breast cancer patients (>1st line). - PerSeus -BC03

PerSeUS:Perpetual Study estimated -by United Sections in Gifu0 sitesStarted: October 7, 2013Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
ot applicable to ot applicable (—)
Sex
Female

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1.Life threatening including large liver metastasis, larege brain metastasis, systematic inflammatory lymphangitis in lung. 2.Inflammatory breast cancer 3.Previous therapy by Fluvestrant. 4.Patients who accetted >4th ET. 5. Allergy to Fluvestrant. 6.Patients considered ineligible by the attending physician.

Investigators

Sponsor
PerSeUS:Perpetual Study estimated -by United Sections in Gifu

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