drugset / Trial / NCT00973245

BAY59-7939 in Atrial Fibrillation Once Daily (OD)

NCT00973245

Phase 2 Completed 102 enrolled Bayer
RandomizedParallel-groupOpen-labelPrevention

Summary

This is an exploratory investigation of safety, pharmacokinetic (PK) and pharmacodynamic (PD) effects of BAY59-7939 with multiple oral doses of 10 mg, 15 mg and 20 mg once daily (od) in Japanese subjects with non-valvular atrial fibrillation (originally described in Japanese).

Timeline

Start
2006-07
Primary completion
Completion
2007-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Rivaroxaban Other / unclassified 10 mg Oral
Subject Rivaroxaban Other / unclassified 15 mg Oral
Subject Rivaroxaban Other / unclassified 20 mg Oral
Comparator Warfarin Small molecule

Indications