Last reviewed · How we verify

Brinavess (Vernakalant)

Medical University of Vienna · FDA-approved active Small molecule

Vernakalant blocks atrial-selective potassium and sodium channels to rapidly restore normal heart rhythm in patients with atrial fibrillation.

Vernakalant blocks atrial-selective potassium and sodium channels to rapidly restore normal heart rhythm in patients with atrial fibrillation. Used for Rapid conversion of recent-onset atrial fibrillation to sinus rhythm.

At a glance

Generic nameBrinavess (Vernakalant)
SponsorMedical University of Vienna
Drug classAtrial-selective antiarrhythmic agent
TargetAtrial potassium channels (Kv1.5, Kv4.3) and sodium channels
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Vernakalant is an atrial-selective antiarrhythmic agent that inhibits multiple ion channels (potassium and sodium channels) with preferential effects on atrial tissue. By blocking these channels, it prolongs the atrial action potential duration and refractory period, thereby suppressing ectopic atrial activity and facilitating conversion of atrial fibrillation to normal sinus rhythm. Its atrial selectivity reduces the risk of ventricular proarrhythmia compared to non-selective antiarrhythmics.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: