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Corvert (IBUTILIDE)

Pfizer · FDA-approved approved Small molecule Quality 60/100

Ibutilide (Corvert), marketed by Pfizer, is a potassium channel blocker indicated for the rapid conversion of atrial fibrillation or atrial flutter, with a key composition patent expiring in 2028. Its primary competitive advantage lies in its specific mechanism of action and FDA approval for rapid conversion, distinguishing it from older off-patent alternatives like amiodarone and bretylium. The primary risk is the increasing competition from generic dofetilide and the upcoming patent expiry of dronedarone in 2031, which may erode market share.

At a glance

Generic nameIBUTILIDE
SponsorPfizer
Drug classAntiarrhythmic
TargetPotassium voltage-gated channel subfamily H member 2
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1995

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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