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Generic Name: dofetilide

Summary for Generic Name: dofetilide

Drug Master File Entries: see list1
Suppliers: see list1
Therapeutic Class:Cardiovascular Agents

Pharmacology for Ingredient: dofetilide

Drug ClassAntiarrhythmic

Clinical Trials for: dofetilide

Study of the Electrocardiographic Effects of Ranolazine, Dofetilide, Verapamil, and Quinidine in Healthy Subjects
Status: Active, not recruiting Condition: Drug-induced Surface ECG Changes

PVI Using Cryoablation Alone in Paroxysmal AtF Patients Converted From Persistent AF With Dofetilide
Status: Recruiting Condition: Persistent AF Converted to Paroxysmal AF or Sinus Rhythm

Using an iPhone ECG to Monitor the QT Interval on Dofetilide and Sotalol Patients
Status: Recruiting Condition: Cardiac Arrhythmia; Qt Interval, Variation in

High Intensity Focused Ultrasound (HIFU) Ablation System Study
Status: Suspended Condition: Atrial Fibrillation

AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibrillation - Pilot Study
Status: Terminated Condition: Atrial Fibrillation; Heart Failure

Catheter Ablation for Recently Diagnosed Paroxysmal Atrial Fibrillation
Status: Recruiting Condition: Atrial Fibrillation

A Study of the Effectiveness of Anti-Arrhythmic Medications After Atrial Fibrillation Ablation
Status: Completed Condition: Atrial Fibrillation

A Comparison of Antiarrhythmic Drug Therapy and Radio Frequency Catheter Ablation in Patients With Paroxysmal Atrial Fibrillation
Status: Completed Condition: Paroxysmal Atrial Fibrillation

Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Patients With Ventricular Tachycardia
Status: Terminated Condition: Defibrillators, Implantable; Tachycardia, Ventricular

Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial
Status: Completed Condition: Atrial Fibrillation; Arrhythmia

Courtesy of ClinicalTrials.org
See more clinical trials for this drug

Applicant Tradename Generic Name Dosage NDA Approval Date Type RLD Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use
CAPSULE;ORAL020931Oct 1, 1999RXYes6,124,363<disabled>
CAPSULE;ORAL020931Oct 1, 1999RXNo6,124,363<disabled>
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