Pilot Randomized Trial With Flecainide in ARVC Patients

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is an inherited arrhythmia disorder
with high risk of ventricular tachycardia or fibrillation, and implantable cardioverter
defibrillator remains as therapy of choice. Antiarrhythmic therapy with different agents
including beta-blockers, sotalol and amiodarone are usually not effective in reducing risk of
arrhythmic events. Recent data indicated that flecainide effectively prevented the
arrhythmias observed in the experimental ARVC animals and in small series of ARVC patients.
These observations provide a strong rationale for conducting a pilot randomized clinical
trial to determine whether flecainide will reduce ventricular arrhythmias in high-risk ARVC
patients. This pilot study is designed as randomized double-blinded placebo-controlled
crossover trial with administration of 100 mg of Flecainide or matching placebo twice a day
for 4 weeks each with a washout period.

Primary specific aim of this pilot trial is to determine whether Flecainide administration is
associated with a significant reduction of number of ventricular ectopic beats (VEBs) in ARVC
patients with implantable cardioverter-defibrillator (ICD).

Secondary specific aims are:

1. to assess safety of flecainide administration with particular emphasis on proarrhythmic
response measured by:

1. VPBs on ECG monitoring,

2. nonsustained and sustained VT/VF episodes documented on ICD interrogation, and

3. effects of Flecainide on QRS morphology and duration.

2. to assess effects of flecainide on burden of VT runs in 7-day ECG recordings.

3. to assess effects of flecainide on burden of atrial premature beats in 7-day recordings.

4. to demonstrate feasibility of enrollment of rare inherited arrhythmia ARVC patients in a
randomized study in the light of planned future large clinical trial with VT/VF/death as
endpoint.

Study population will include 38 ARVC patients diagnosed with the 2010 ARVC Task Force
Criteria who are at least 18 years old, have implanted ICD, and show at least 500 VPBs in a
24-hour Holter recording. Patients on other pharmacological antiarrhythmic treatment other
than beta-blockers and patients with prior catheter VT ablation will be excluded.

Inclusion Criteria:

- Age > 18 years.

- Subjects who have been diagnosed with ARVC and meet 2010 Modified Task Force Criteria
for ARVC as affected.

- At minimum 500 VPBs on the most recent 24-hour Holter monitor recording prior to
consent or after consent if a subsequent recording is required after 5 day washout
following discontinuation of anti-arrhythmic medication.

- Functioning implanted cardioverter defibrillator with remote interrogation capability.

- Subjects should be on a beta-blocker including metoprolol, propranolol, atenolol,
nadolol, carvedilol or bisoprolol unless contraindication to beta-blockers exists.

- Persons prescribed quinidine, procainamide, propafenone, disopyramide, dronedarone
phenytoin, mexilitene, flecainide, may be included after 5 day washout period with
subsequent 24 Hour Holter obtained after washout period.

- Persons prescribed sotalol must be included after 5 day washout period during which
another beta-blocker may be administered with subsequent 24 Hour Holter obtained.

- Subject and personal physician and or cardiologist must agree not to use any
antiarrhythmic medications during the 10 weeks of participation, unless needed for
management of life-threatening arrhythmias.

- All subjects must agree to use medically acceptable contraceptive measures during
participation unless documented as surgically sterile or post-menopausal (no menstrual
periods for more than one year).

Exclusion Criteria:

- Prescribed amiodarone or dofetilide at the time of consent.

- Left ventricular ejection fraction ≤40% by any imaging modality: echocardiography,
angiography, CMRI, or cardiac nuclear test on the most recent test.

- NYHA heart failure class III or IV at time of consent.

- Prior myocardial infarction at any time in the past.

- Pacemaker dependent rhythm at the time of consent.

- Renal impairment (GFR <30 mL/min/m2).

- Prior diagnosis of severe hepatic impairment.

- Pregnant or plan to become pregnant during the course of the trial (Flecainide has not
been adequately studied in pregnant women). Pregnancy test is required for women of
child-bearing potential prior to randomization.

- Participating in any other interventional clinical trial.

- Unwilling or unable to cooperate with the protocol.

- Lives at such a distance from the clinic that travel for the consent visit would be
unusually difficult.

- Decisionally impaired adults, those of questionable capacity, those who cannot manage
taking the study drug per the prescribed regimen, and those who cannot consent for
themselves will not be recruited for this study.

- Unwilling to sign the consent for participation.