Safety and tolerability of an immediate-release formulation of the oral direct thrombin inhibitor AZD0837 in the prevention of stroke and systemic embolism in patients with atrial fibrillation

Bertil S. Olsson; Lars H. Rasmussen; Arnljot Tveit; Eva Jensen; Peter Wessman; Seva Panfilov; Karin Wåhlander

doi:10.1160/TH09-07-0509

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2010; 103(03): 604-612
DOI: 10.1160/TH09-07-0509

Blood Coagulation, Fibrinolysis and Cellular Haemostasis

Schattauer GmbH

Safety and tolerability of an immediate-release formulation of the oral direct thrombin inhibitor AZD0837 in the prevention of stroke and systemic embolism in patients with atrial fibrillation

Bertil S. Olsson

¹Department of Cardiology, Lund University Hospital, Sweden

,

Lars H. Rasmussen

²Department of Cardiology, Aalborg Hospital, Aarhus University Hospital, Denmark

,

Arnljot Tveit

³Department of Internal Medicine, Asker and Baerum Hospital, Norway

,

Eva Jensen

⁴AstraZeneca R&D, Mölndal, Sweden

,

Peter Wessman

⁴AstraZeneca R&D, Mölndal, Sweden

,

Seva Panfilov

⁴AstraZeneca R&D, Mölndal, Sweden

,

Karin Wåhlander

⁴AstraZeneca R&D, Mölndal, Sweden

› Author Affiliations

Abstract

Summary

AZD0837 is an investigational oral anticoagulant which is converted to the active form, AR-H067637, a selective direct thrombin inhibitor. The present study, a multicentre, randomised, parallel-group, dose-guiding study, assessed the safety and tolerability of an immediate-release formulation of AZD0837 compared with dose-adjusted warfarin in the prevention of stroke and systemic embolic events in atrial fibrillation (AF) patients. Two hundred fifty AF patients with at least one additional risk factor for stroke were randomised to receive either immediate-release AZD0837 (150 mg twice daily [bid] or 350 mg bid, blinded treatment) or dose-adjusted warfarin (international normalised ratio 2.0–3.0, open treatment) for three months. The safety and tolerability of 150 mg bid AZD0837 appeared to be as good as that of warfarin. Total bleeding events were six with 150 mg bid AZD0837, 15 with 350 mg bid AZD0837 and eight with warfarin. Alanine aminotransferase elevations (> 3 x upper limit of normal) were infrequent, without apparent differences between treatment groups. A numerically higher incidence of serious adverse events was observed with 350 mg bid AZD0837 compared with 150 mg bid, with six of 13 being cardiac related, all with different diagnoses. An increase in mean serum creatinine of approximately 10% was observed in both AZD0837 groups, which returned to baseline after completion of therapy. There were no strokes, transient ischaemic attacks or cerebral haemorrhages with any of the treatments. In conclusion, the safety and tolerability of 150 mg bid immediate-release AZD0837 appeared to be as good as that of dose-adjusted warfarin. However, larger studies will be needed to define the safety profile of AZD0837.

Keywords

Stroke - atrial fibrillation - anticoagulant - oral direct thrombin inhibitor - AZD0837

Full Text

References

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