| Literature DB >> 33512711 |
Mendy Ter Avest1, Saskia M C Langemeijer2, Saskia E M Schols2, David M Burger1, Nicole C A J van de Kar3, Nicole M A Blijlevens2, Wietske Kievit4, Rob Ter Heine1.
Abstract
Ravulizumab is a very expensive complement C5-inhibitor for the treatment of paroxysmal nocturnal haemoglobinuria, with a fixed-dosing interval of 8 weeks. For lifelong treatment, a cost-effective and patient-friendly dosing strategy is preferred. We therefore explored alternative ravulizumab dosing regimens in silico based on the thorough dose-finding studies of the manufacturer. Extending the interval to 10 weeks or individually extending the interval to a mean of 12.8 weeks based on pharmacokinetic monitoring resulted in noninferior efficacy in terms of lactate dehydrogenase normalization, with drug cost savings up to 37%. We here show the potential of individualized ravulizumab dosing to improve patient-friendliness at reduced costs.Entities:
Keywords: paroxysmal nocturnal haemoglobinuria; pharmacodynamics; pharmacokinetics; ravulizumab
Year: 2021 PMID: 33512711 DOI: 10.1111/bcp.14748
Source DB: PubMed Journal: Br J Clin Pharmacol ISSN: 0306-5251 Impact factor: 4.335