drugset / Trial / NCT04636632

Fosaprepitant for the Prevention of Nausea and Emesis During Concurrent Chemoradiotherapy for Nasopharyngeal Carcinoma

NCT04636632

Phase 1 Completed 100 enrolled Sun Yat-sen University
RandomizedParallel-groupOpen-labelPrevention

Summary

This is an opene-label, single center, randomized prospective pilot study to compare the efficacy of weekly versus triweekly fosaprepitant regimens for the prevention of nausea and emesis during concurrent chemoradiotherapy for nasopharyngeal carcinoma (NPC).

Timeline

Start
2020-11-24
Primary completion
2022-11-04
Completion
2022-11-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosaprepitant Other / unclassified 150 mg/m2