drugset / Trial / NCT01661335

Efficacy of Aprepitant (Emend®) in Children

NCT01661335

Phase 3 Completed 19 enrolled University of Oklahoma
RandomizedCrossoverTriple-blindPrevention

Summary

The purpose of this study is to find out whether or not adding aprepitant(Emend®) to the standard therapy will help children who receive chemotherapy to have less nausea and vomiting.

Timeline

Start
2012-06-01
Primary completion
2017-06-29
Completion
2017-06-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Aprepitant Other / unclassified 2 mg/kg Oral
Subject Dexamethasone Small molecule 0.2 mg/kg Intravenous
Subject Dexamethasone Small molecule 0.4 mg/kg Intravenous
Background Ondansetron Other / unclassified 0.15 mg/kg Intravenous