drugset / Trial / NCT01405924

Fosaprepitant (MK-0517, EMEND® IV) In Salvage Treatment of Chemotherapy-Induced Vomiting (MK-0517-030)

NCT01405924

Phase 2 Terminated 111 enrolled Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelPrevention

Summary

This study will assess the efficacy of a single dose of intravenous (IV) fosaprepitant (MK-0517, EMEND® IV) as salvage therapy when added to a 5-hydroxytryptamine receptor 3 antagonist (5-HT3 RA) and dexamethasone for the prevention of chemotherapy-induced vomiting (CIV) in participants who experienced CIV in the first cycle of moderately emetic chemotherapy (MEC). The primary hypothesis is that there will be no vomiting and no retching in at least 20% of participants during the second cycle of MEC in participants who previously experienced vomiting during the first cycle of MEC.

Timeline

Start
2011-10-25
Primary completion
2013-12-06
Completion
2013-12-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosaprepitant Other / unclassified 150 mg Intravenous
Background Dexamethasone Small molecule

Indications

No indication recorded.