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Clinical Trial Summary

The purpose of this study is to determine response rates by administering low dose cyclophosphamide on day 1, followed by 5 days of outpatient IL2.


Clinical Trial Description

To determine the response rate, median duration of response and median survival of patients treated with this low-dose cyclophosphamide + moderate dose bolus Interleukin-2 schedule. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01833767
Study type Interventional
Source Western Regional Medical Center
Contact
Status Withdrawn
Phase Phase 2
Start date October 2012
Completion date December 2015

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