drugset / Trial / NCT00267930

Study of RSD1235-SR for the Prevention of Atrial Fibrillation/Atrial Flutter Recurrence

NCT00267930

Phase 2 Completed 221 enrolled Advanz Pharma
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study is designed to evaluate the safety, tolerability and preliminary efficacy of vernakalant (oral) in subjects with sustained atrial fibrillation of greater than 72 hours and less than 6 months duration

Timeline

Start
2005-12
Primary completion
Completion
2006-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Vernakalant Other / unclassified 300 mg Oral
Subject Vernakalant Other / unclassified 600 mg Oral

Indications