drugset / Trial / NCT00468767

Phase III Tolerance and Efficacy Study of RSD1235 in Patients With Atrial Fibrillation

NCT00468767 ↗

Phase 3 Completed 356 enrolled Advanz Pharma Astellas Pharma US, Inc. · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is being conducted to demonstrate the effectiveness of RSD1235 in the conversion of atrial fibrillation to sinus rhythm.

Timeline

Start
2003-08
Primary completion
2004-11
Completion
2004-11

Outcome

Met primary endpoint

paper 75 (51.7%) in the short-duration AF group converted to sinus rhythm (median time, 11 minutes) compared with 3 of the 75 placebo patients (4.0%; P<0.001). PMID 18332267 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Vernakalant Other / unclassified 3 mg/kg Intravenous

Indications