NDAINJECTIONINJECTABLE
Approved
Dec 1995
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
3/8 — Basic
CORVERT (ibutilide fumarate) by Pfizer is mechanism of action: corvert injection prolongs action potential duration in isolated adult cardiac myocytes and increases both atrial and ventricular refractoriness in vivo , ie, class iii electrophysiologic effects. First approved in 1995.
Drug data last refreshed 3h ago · AI intelligence enriched 1mo ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
CORVERT (ibutilide fumarate) is an intravenous Class III antiarrhythmic agent approved in 1995 for acute conversion of atrial fibrillation and atrial flutter. It works by prolonging action potential duration and refractoriness through activation of a slow, inward sodium current, a unique mechanism among Class III agents. CORVERT is administered as a short IV infusion in acute care settings.
LOE Approaching
Product approaching loss of exclusivity with moderate competitive pressure (30/100); brand team likely in maintenance and generic defense mode with reduced headcount.
Mechanism of Action
Mechanism of Action: CORVERT Injection prolongs action potential duration in isolated adult cardiac myocytes and increases both atrial and ventricular refractoriness in vivo , ie, class III electrophysiologic effects. Voltage clamp studies indicate that CORVERT, at nanomolar concentrations, delays…
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
CORVERT offers limited career growth as a LOE-stage product with minimal linked job openings and declining commercial investment. Roles remain primarily in commercial defense, hospital access, and reimbursement management rather than innovation or expansion.
Brand Manager
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.