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Clinical Trial Summary

Difluoromethylornithine (DFMO) will be used in an open label, single agent, multicenter, study for patients with neuroblastoma in remission. In this study subjects will receive 730 Days of oral difluoromethylornithine (DFMO) at a dose of 750 mg/m2 ± 250 mg/m2 BID (strata 1, 2, 3, and 4) OR 2500 mg/m2 BID (stratum 1B) on each day of study. This study will focus on the use of DFMO in high risk neuroblastoma patients that are in remission as a strategy to prevent recurrence.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02679144
Study type Interventional
Source Milton S. Hershey Medical Center
Contact Genevieve Bergendahl, MSN
Phone 7175310003
Email gbergendahl@pennstatehealth.psu.edu
Status Recruiting
Phase Phase 2
Start date February 2016
Completion date February 2033

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