Ivabradine
Approved · EMAAlso known as Corlanor, Ivabradin, Ivabradina, Ivabradinum.
Recent clinical, regulatory, research and industry developments relating to this drug.
Heart Rate Control: Betablockers or Ivabradine Therapy Before Cardiac Computed Tomography
Approval: Ivabradine Anpharm (EMA)
Drug Safety Update: Ivabradine: carefully monitor for bradycardia
Ivabradine in stable coronary artery disease without clinical heart failure.
Single centre experience of ivabradine in postural orthostatic tachycardia syndrome.
Profile
Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.
Regulatory timeline
The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.
Indication: Symptomatic treatment of chronic stable angina pectoris Ivabradine is indicated for the symptomatic treatment of chronic stable angina pectoris in coronary artery disease adults… Show full indicationShow less
Symptomatic treatment of chronic stable angina pectoris Ivabradine is indicated for the symptomatic treatment of chronic stable angina pectoris in coronary artery disease adults with normal sinus rhythm and heart rate ? 70 bpm. Ivabradine is indicated: in adults unable to tolerate or with a contra-indication to the use of beta-blockers or in combination with beta-blockers in patients inadequately controlled with an optimal betablocker dose. Treatment of chronic heart failure Ivabradine is indicated in chronic heart failure NYHA II to IV class with systolic dysfunction, in patients in sinus rhythm and whose heart rate is ? 75 bpm, in combination with standard therapy including beta-blocker therapy or when beta-blocker therapy is contraindicated or not tolerated.
Data from the U.S. Food and Drug Administration (U.S. Food and Drug Administration), public domain (CC0).
Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.
Contains public sector information from the Medicines and Healthcare products Regulatory Agency (MHRA) licensed under the Open Government Licence (OGL v3).
Clinical trials
The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.
Late-stage studies
Phase III+ trials still open or recently active — where late-stage evidence is being generated.
Pulse Reduction On Beta-blocker and Ivabradine Therapy
Recent completions
Trials that read out recently, adding to the completed evidence base.
Pulse Reduction On Beta-blocker and Ivabradine Therapy
Research activity
Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.
Journals, researchers & institutions
- Lancet (London, England)3
- Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2
- American heart journal1
- Rambam Maimonides medical journal1
- The New England journal of medicine1
- Ford I5
- Ferrari R3
- Fox K3
- Steg PG3
- Tendera M3
- Böhm M2
- Borer JS2
- Dubost-Brama A2
- From the National Heart and Lung Institute1
- Institute for Ageing and Health1
- Institute for Cellular Medicine1
- J. Recanati Autonomic Dysfunction Center1
- NHLI Imperial College and ICMS Royal Brompton Hospital1
- Royal Brompton Hospital1
- RxNorm (U.S. National Library of Medicine) — drug identity
- ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
- Europe PMC — research literature
- ClinicalTrials.gov — clinical trials
- Regulatory event sources are credited in the Regulatory Timeline above.