Preemptive treatment of Cytomegalovirus infection in kidney transplant recipients with letermovir: results of a Phase 2a study. (January 2014)

• Record Type: Journal Article
• Authors: Stoelben, Susanne; Arns, Wolfgang; Renders, Lutz; Hummel, Jürgen; Mühlfeld, Anja; Stangl, Manfred; Fischereder, Michael; Gwinner, Wilfried; Suwelack, Barbara; Witzke, Oliver; Dürr, Michael; Beelen, Dietrich W.; Michel, Detlef; Lischka, Peter; Zimmermann, Holger; Rübsamen‐Schaeff, Helga; Budde, Klemens
• Is Part Of: Transplant international. Volume 27:Number 1(2014:Jan.)
• Page Start: 77
• Page End: 86
• Publication Date: 2014-01
• Subjects: Transplantation of organs, tissues, etc -- Periodicals; 617.95405
• DOI: 10.1111/tri.12225
• Languages: English
• ISSNs: 0934-0874

Abstract

<abstract abstract-type="main" id="tri12225-abs-0001"> <title>Summary</title> <p>Cytomegalovirus (CMV) infection remains a significant cause of morbidity and mortality in transplant recipients. Letermovir (AIC246), is a novel anti‐HCMV drug in development, acting via a novel mechanism of action. In this proof‐of‐concept trial with first administration of letermovir to patients, 27 transplant recipients with active CMV replication were randomly assigned to a 14‐day oral treatment regimen of either letermovir 40 mg twice a day, letermovir 80 mg once a day, or local standard of care (SOC) in a multicenter, open‐label trial. Efficacy, safety, and limited pharmacokinetic parameters were assessed. All groups had a statistically significant decrease in CMV‐DNA copy number from baseline (40 mg BID: <italic>P</italic> = 0.031; 80 mg QD: <italic>P</italic> = 0.018; SOC: <italic>P</italic> = 0.001), and comparison of viral load reduction between treatment groups showed no statistically significant differences. Viral clearance was achieved for 6 of 12 patients (50%) in the letermovir groups versus two of seven SOC patients (28.6%). Letermovir treatment was generally well tolerated, no patient developed CMV disease during the trial. Both letermovir treatment regimens resulted in equally high trough level plasma concentrations. The efficacy, safety, and pharmacokinetics observed in these viremic transplant recipients indicate that letermovir is a promising new anti‐CMV drug.</p> </abstract>