drugset / Trial / NCT00623779

Atrial Fibrillation (AF) Patients Not Taking Vitamin-K Antagonist (VKA)

NCT00623779

Phase 2 Completed 128 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to assess the safety and tolerability of AZD0837 in patients with atrial fibrillation who are unable or unwilling to take vitamin K antagonist therapy for up to 3 months.

Timeline

Start
2007-10
Primary completion
2008-10
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Subject ATECEGATRAN METOXIL Small molecule Oral
Subject Aspirin Small molecule Oral