Drug data last refreshed 18h ago · AI intelligence enriched 3w ago
CORLANOR (ivabradine) is an oral small-molecule tablet approved in 2015 by the FDA for treating symptomatic chronic heart failure in adult patients with left ventricular ejection fraction ≤35% to reduce hospitalization for worsening heart failure. It works by selectively inhibiting the hyperpolarization-activated cyclic nucleotide-gated (HCN) channel responsible for the cardiac pacemaker I_f current, thereby reducing heart rate without affecting myocardial contractility. The drug is indicated for patients already on maximally tolerated doses of beta-blockers, positioning it as an add-on therapy in advanced heart failure management.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Ivabradine Effects in Cardiogenic Shock Requiring Inotropic Support
An Interventional Study to Evaluate the Effect of Ivabradine on Exercise Capacity in Heart Transplant Recipients
Trial Assessing the Effectiveness of Ivabradine Started at Discharge From the Observation Unit
Effect of Ivabradine in Stage D HF/Cardiogenic Shock Patients on Dobutamine
Ivabradine in the Management of Cardiac Autonomic Dysfunction Associated With Thoracic Radiation Therapy.
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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.
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CORLANOR supports specialized roles including heart failure brand managers, medical science liaisons targeting cardiologists, and field representatives focused on hospital formulary positioning and heart failure specialists. Success in this role requires deep cardiology knowledge, understanding of heart failure guidelines, and ability to position the drug within complex treatment algorithms for advanced HF patients. Currently, zero job openings are linked to this product in the available data, reflecting mature post-launch status and anticipated near-term generic competition.