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
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Primary completion
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Completion
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Drugs

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