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Clinical Trial Summary

This is an open label, Phase II, multi-center study designed to evaluate the effect of AVR118 when administered to patients with systemic symptoms related to recurrent or metastatic cancers who may or may not be undergoing anti-cancer treatment. During the initial, induction treatment phase of the study, AVR118, 4.0 mL, will be given subcutaneously each day for 28 days. Patients who respond to the trial period dosing will be eligible to continue on AVR118 if they and their physicians believe it would be beneficial, and if no safety concerns are raised.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00765466
Study type Interventional
Source McGill University
Contact
Status Terminated
Phase Phase 2
Start date October 2007
Completion date May 2010

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