drugset / Trial / NCT00751738

Long Term Safety of 125 mg Per Day of Oral Azimilide in Patients With Implantable Cardioverter Defibrillator (ICDs)

NCT00751738

Phase 3 Completed 330 enrolled Forest Laboratories
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multi-center, long-term, (open-ended) safety study with 125 mg per day of azimilide in patients who completed protocol 2000098.

Timeline

Start
2002-10
Primary completion
2005-10
Completion
2005-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Azimilide Small molecule 125 mg Oral