drugset / Trial / NCT02106494

A Prospective, Multicenter, Study of APF530 (Granisetron) SC for Prevention of CINV in Patients Receiving HEC

NCT02106494

Phase 3 Completed 942 enrolled Heron Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary study objective is to demonstrate the superiority of APF530 500 mg given subcutaneously (SC) compared with ondansetron 0.15 mg/kg given intravenously (IV) (up to a maximum of 16 mg) in the delayed-phase (\> 24-120 hours) complete response (CR) rate (defined as no emesis and no use of rescue medications) in subjects receiving highly emetogenic chemotherapy (HEC) as defined by the 2011 ASCO CINV guidelines

Timeline

Start
2014-03
Primary completion
2015-05
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Granisetron Other / unclassified 10 mg Subcutaneous
Comparator Ondansetron Other / unclassified 0.15 mg/kg Intravenous
Background Dexamethasone Small molecule 12 mg Intravenous
Background Fosaprepitant Other / unclassified 150 mg Intravenous