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Clinical Trial Summary

The investigators developed a protocol utilizing once-daily intravenous busulfan/melphalan/etoposide regimen as a conditioning for high-dose therapy (HDT) in the patients with high risk or relapsed Non-Hodgkin's Lymphoma (NHL).


Clinical Trial Description

Treatment:

busulfan 3.2 mg/kg/day i.v. on day -7, -6, and -5 etoposide 400 mg/m2 i.v. on day -5 and -4 melphalan 50mg/m2/day i.v. on day -3 and -2 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03792815
Study type Interventional
Source Soonchunhyang University Hospital
Contact
Status Completed
Phase Phase 2
Start date October 2009
Completion date September 2013

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