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

Outcome

Missed primary endpoint

paper there was no statistically significant difference in the complete response primary end point PMID 37498596 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosaprepitant Other / unclassified 150 mg/m2 —