drugset / Trial / NCT00539591

Phase II Study Incorporating Pegylated Interferon In the Treatment For Children With High-Risk Melanoma

NCT00539591

Phase 2 Active not recruiting 29 enrolled St. Jude Children's Research Hospital Schering-Plough · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main goal of this study is to estimate the tumor response rate of temozolomide administered in combination with peginterferon alfa-2b to pediatric patients with unresectable Stage III, metastatic, or recurrent cutaneous melanoma.

Timeline

Start
2008-05-09
Primary completion
2015-06
Completion
2031-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Peginterferon alfa-2b Protein / enzyme biologic 0.5 ug/kg Intravenous
Subject Peginterferon alfa-2b Protein / enzyme biologic 1 ug/kg Intravenous
Subject Peginterferon alfa-2b Protein / enzyme biologic 2e+07 unknown Intravenous
Subject Temozolomide Small molecule 75 mg/m2 Oral

Indications