drugset / Trial / NCT01518413

Dose Escalation Study of Sorafenib and Irinotecan Combination Therapy in Pediatric Patients With Solid Tumors

NCT01518413 ↗

Phase 1 Completed 17 enrolled HMeany
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safest and most effective oral dose combinations of sorafenib and irinotecan in pediatric patients with solid tumors, i.e. relapsed or refractory.

Timeline

Start
2011-12
Primary completion
2015-01
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Irinotecan Small molecule 70 mg/m2 Oral
Subject Sorafenib Small molecule 150 mg/m2 Oral