drugset / Trial / NCT00666783

An Efficacy and Safety Study of Palonosetron in Preventing Chemotherapy-Induced Nausea and Vomiting (CINV) in the Chinese Cancer Patients

NCT00666783

Phase 2 Completed 208 enrolled Xijing Hospital
RandomizedParallel-groupDouble-blindSupportive care

Summary

This clinical study was designed to demonstrate that a single, intravenous dose of palonosetron 0.25 mg was not inferior to granisetron 3 mg in preventing acute and delayed CINV and was also well tolerated in the Chinese cancer patients.

Timeline

Start
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Granisetron Other / unclassified 3 mg Intravenous
Subject Palonosetron Other / unclassified 0.25 mg Intravenous