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Clinical Trial Summary

This study is designed as an open-label randomized parallel two-arm multicenter efficacy, pharmacokinetics and safety study of intravenously administered eribulin versus intravenously administered vinorelbine in Chinese population. Eligible female subjects will have measurable disease according to RECIST 1.1 with the modification that chest x-ray cannot be used for assessment of disease.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02225470
Study type Interventional
Source Eisai Inc.
Contact
Status Active, not recruiting
Phase Phase 3
Start date September 26, 2013
Completion date March 2018

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