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Monotherapy With Eribulin In Her2 Negative Metastatic Breast Cancer as a First Line Treatment — MERIBEL  

Breast Neoplasm Clinical Trial

Official title:
A Phase IIa Prospective, Multicenter, Open and Not Controlled of the Efficacy and Tolerability on the First Line Treatment With Eribulin as a Unic Agent on Patients With HER2 Negative Metastatic Breast Cancer Previously Treated With Taxanes

Clinical Trial Summary

Multicentre, prospective, non-controlled phase II clinical trial to evaluate the efficacy and tolerability of first line single agent Eribulin in patients with HER2-negative metastatic breast carcinoma previously exposed to taxanes for early stage. The primary objective of the study is to determine the median time to progression achieved with Eribulin. Other secondary objectives will be; overall response rate, clinical benefit rate, time to treatment progression, duration of response and toxicity profile.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02061085
Study type Interventional
Source MedSIR
Contact
Status Completed
Phase Phase 2
Start date July 2013
Completion date December 2015
View Details
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