drugset / Trial / NCT00388726

E7389 Versus Treatment of Physician's Choice in Patients With Locally Recurrent or Metastatic Breast Cancer

NCT00388726 ↗

Phase 3 Completed 762 enrolled Eisai Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare Overall Survival (OS), Progression Free Survival (PFS), objective tumor response rate, duration of response, and safety in patients treated with E7389 versus the Treatment of Physician's Choice (TPC) in patients with locally recurrent or metastatic breast cancer.

Timeline

Start
2006-11
Primary completion
2009-05
Completion
2013-06

Outcome

Met primary endpoint

paper Overall survival was significantly improved in women assigned to eribulin PMID 21376385 ↗

release “The EMBRACE Study met its primary endpoint of demonstrating a statistically significant improvement in overall survival in eribulin-treated patients compared to treatment of physician's choice.” eisai.com ↗

release “EMBRACE Study demonstrated that patients treated with Halaven® survived a median of 2.5 months longer” eisai.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Eribulin Small molecule 1.4 mg/m2 Intravenous

Indications