Thromb Haemost 2015; 113(04): 719-727
DOI: 10.1160/TH14-06-0547
Coagulation and Fibrinolysis
Schattauer GmbH

Pharmacokinetics, safety, and tolerability of edoxaban in end-stage renal disease subjects undergoing haemodialysis

Dolly A. Parasrampuria
1   Daiichi Sankyo Pharma Development, Edison, New Jersey, USA
,
Thomas Marbury
2   Orlando Clinical Research Center, Orlando, Florida, USA
,
Nobuko Matsushima
3   Daiichi Sankyo Co, Ltd., Tokyo, Japan
,
Shuquan Chen
1   Daiichi Sankyo Pharma Development, Edison, New Jersey, USA
,
Prachi K. Wickremasingha
4   Certified Consultant Pharmacists Inc., Chatham, New Jersey, USA
,
Ling He
1   Daiichi Sankyo Pharma Development, Edison, New Jersey, USA
,
Victor Dishy
1   Daiichi Sankyo Pharma Development, Edison, New Jersey, USA
,
Karen S. Brown
1   Daiichi Sankyo Pharma Development, Edison, New Jersey, USA
› Author Affiliations
Further Information

Publication History

Received: 23 June 2014

Accepted after major revision: 05 January 2014

Publication Date:
24 November 2017 (online)

Summary

Edoxaban is an oral, direct, once-daily, factor Xa inhibitor developed for stroke prevention in patients with atrial fibrillation and for the treatment and secondary prevention of recurrent thromboembolism in patients with acute symptomatic venous thromboembolism. Among elderly patients who require anticoagulation therapies, some may have end-stage renal disease (ESRD). This open-label, phase 1, randomised, two-way crossover study was conducted to evaluate the pharmacokinetics of edoxaban in 10 subjects on haemodialysis. Eligible subjects with ESRD on chronic haemodialysis received a single, oraldose of edoxaban 15 mg 2 hours (h) prior to (on-dialysis) or in between (off-dialysis) haemodialysis sessions. Haemodialysis resulted in a minor decrease in mean total exposure (AUC0-∞; 676.2 ng⋅h/ml) as compared with that observed in subjects off-dialysis (691.7 ng⋅h/ml). Mean maximum observed plasma concentration (Cmax) values were comparable between on-dialysis and off-dialysis treatments (53.3 vs 56.3 ng/ml, respectively). Mean apparent total body clearance (CL/F) values were 24.1 and 22.5 l/h during the on-dialysis and off-dialysis treatment periods, respectively. Dialyser clearance was 5.7 l/h and haemodialysis clearance was 6.1 l/h. Haemodialysis clearance was only 6.1 l/h, suggesting that it only accounts for one-fourth of the total clearance in these subjects. A single, oral dose of 15 mg of edoxaban was well tolerated by subjects with ESRD. In conclusion, based on these single-dose PK data, a supplementary dose of edoxaban may not be required following a haemodialysis session. Importantly, haemodialysis is not an effective mechanism for removal of edoxaban from the blood.

 
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