A Study of LY573636-sodium in Patients With Metastatic Breast Cancer

Status Completed

Clinical Trial Summary

The primary purpose of this study is to determine the objective response rate (complete and partial response) for patients who receive LY573636-sodium for metastatic breast cancer.

Clinical Trial Description

Patient will receive a 2-hour intravenous infusion of study drug (LY573636-sodium) once every 28 days. Radiologic imaging scans will be performed before the first dose of study drug and then after every other treatment. Patients will be assessed for clinical progression at every visit and for response approximately every 56 days (every other cycle). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00992225
Study type	Interventional
Source	Eli Lilly and Company
Contact
Status	Completed
Phase	Phase 2
Start date	September 2009
Completion date	April 2011

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