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A Study of LY573636-Sodium in the Treatment of Patients With Metastatic Soft Tissue Sarcoma

Sarcoma, Soft Tissue Clinical Trial

Official title:
A Phase 2 Study of LY573636-Sodium Administered as Second-line or Third-line Treatment in Patients With Unresectable or Metastatic Soft Tissue Sarcoma

Clinical Trial Summary

The primary purpose of the study is to estimate the time from the first dose of LY573636-sodium (hereafter referred to as LY573636) to the date your physician determines that your disease has progressed or worsened.

Clinical Trial Description

Patients will receive a 2-hour intravenous infusion of study drug (LY573636) once every 21 days or 28 days depending on their target dose. Radiological 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 42 days or 56 days (every other cycle). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00490451
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 2
Start date August 2007
Completion date February 2010
View Details
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