drugset / Trial / NCT03674294

Aprepitant Triple Therapy for the Prevention of CINV in Nondrinking and Young Women Who Received Moderately Emetogenic Chemotherapy

NCT03674294

Phase 3 Completed 248 enrolled Sun Yat-sen University
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to study whether adding Aprepitant to Palonosetron and dexamethasone can further prevent the incidence and severity of nausea and vomiting caused by FOLFIRI or FOLFOX chemotherapy regimen among gastrointestinal malignancy patients with high risk factors of chemotherapy-associated adverse events.

Timeline

Start
2015-08-04
Primary completion
2020-03-31
Completion
2020-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Aprepitant Other / unclassified 80 mg Oral
Subject Dexamethasone Small molecule 6 mg Oral
Subject Dexamethasone Small molecule 12 mg Oral
Background Palonosetron Other / unclassified 0.25 mg Intravenous