Your browser doesn't support javascript.
loading
Dissociation between the pharmacokinetics and pharmacodynamics of once-daily rivaroxaban and twice-daily apixaban: a randomized crossover study.
Kreutz, R; Persson, P B; Kubitza, D; Thelen, K; Heitmeier, S; Schwers, S; Becka, M; Hemmrich, M.
Afiliação
  • Kreutz R; Institut für Klinische Pharmakologie und Toxikologie, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Persson PB; Institut für Vegetative Physiologie, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Kubitza D; Bayer AG, Wuppertal, Germany.
  • Thelen K; Bayer AG, Wuppertal, Germany.
  • Heitmeier S; Bayer AG, Wuppertal, Germany.
  • Schwers S; Bayer AG, Wuppertal, Germany.
  • Becka M; Bayer AG, Wuppertal, Germany.
  • Hemmrich M; Bayer AG, Berlin, Germany.
J Thromb Haemost ; 15(10): 2017-2028, 2017 10.
Article em En | MEDLINE | ID: mdl-28805299
ABSTRACT
Essentials In this crossover study the anticoagulant effects of rivaroxaban and apixaban were compared. Healthy volunteers received rivaroxaban 20 mg once daily or apixaban 5 mg twice daily. Rivaroxaban was associated with more prolonged inhibition of thrombin generation than apixaban. Rivaroxaban induced a clear prolongation of prothrombin time and activated partial thromboplastin time.

SUMMARY:

Background The anticoagulant actions of the oral direct activated factor Xa inhibitors, rivaroxaban and apixaban, have not previously been directly compared. Objectives To compare directly the steady-state pharmacokinetics and anticoagulant effects of rivaroxaban and apixaban at doses approved for stroke prevention in patients with non-valvular atrial fibrillation. Methods Twenty-four healthy Caucasian male volunteers were included in this open-label, two-period crossover, phase 1 study (EudraCT number 2015-002612-32). Volunteers were randomized to receive rivaroxaban 20 mg once daily or apixaban 5 mg twice daily for 7 days, followed by a washout period of at least 7 days before they received the other treatment. Plasma concentrations and anticoagulant effects were measured at steady state and after drug discontinuation. Results Overall exposure was similar for both drugs the geometric mean area under the plasma concentration-time curve for the 0-24-h interval was 1830 µg h L-1 for rivaroxaban and 1860 µg h L-1 for apixaban. Rivaroxaban was associated with greater inhibition of endogenous thrombin potential (geometric mean area under the curve relative to baseline during the 0-24-h interval 15.5 h versus 17.5 h) and a more pronounced maximal prolongation relative to baseline of prothrombin time (PT) (1.66-fold versus 1.14-fold) and activated partial thromboplastin time (APTT) (1.43-fold versus 1.16-fold) at steady state than apixaban. Conclusions Despite similar exposure to both drugs, rivaroxaban 20 mg once daily was associated with greater and more sustained inhibition of thrombin generation than apixaban 5 mg twice daily. Sensitive PT and APTT assays can be used to estimate the anticoagulant effects of rivaroxaban.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirazóis / Piridonas / Coagulação Sanguínea / Inibidores do Fator Xa / Rivaroxabana Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: J Thromb Haemost Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirazóis / Piridonas / Coagulação Sanguínea / Inibidores do Fator Xa / Rivaroxabana Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: J Thromb Haemost Ano de publicação: 2017 Tipo de documento: Article