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Thromb Haemost 2006; 95(03): 447-453
DOI: 10.1160/TH05-10-0664
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Antithrombotic effects of ximelagatran plus acetylsalicylic acid (ASA) and clopidogrel plus ASA in a human ex vivo arterial thrombosis model

Karin Wåhlander
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
Maria Eriksson-Lepkowska
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
Per Nyström
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
Ulf G. Eriksson
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
Troy C. Sarich
2   AstraZeneca LP, Wilmington, Delaware, USA
,
Juan J. Badimon
3   Cardiovascular Institute, Mount Sinai School of Medicine, New York, USA
,
Inge Kalies
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
Margareta Elg
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
Anders Bylock
1   AstraZeneca R&D Mölndal, Mölndal, Sweden
› Author Affiliations
Further Information

Publication History

Received 10 October 2005

Accepted after resubmission 12 January 2006

Publication Date:
29 November 2017 (online)

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Summary

It was the objective of this study to compare the antithrombotic effects and bleeding profiles of the oral direct thrombin inhibitor ximelagatran, an anticoagulant, and the antiplatelet agent clopidogrel on top of steady-state acetylsalicylic acid (ASA) in a human arterial thrombosis model. Healthy male volunteers (n=62) received ASA (160 mg once daily),plus either clopidogrel for 6 days (loading dose 300 mg, then 75 mg once daily), or a single dose of ximelagatran (36 or 72 mg) on Day 6. Changes in total thrombus area (TTA) under low shear rate (LSR; 212 s-1) and high shear rate (HSR; 1690 s-1) conditions were measured, using the ex vivo Badimon perfusion chamber model pre-dose and 2 and 5 hours after dosing on Day 6, and capillary bleeding times (CBT) were determined. Ximelagatran plus ASA significantly reduced TTA under LSR and HSR, compared with ASA alone. Ximelagatran plus ASA reduced TTA more than clopidogrel plus ASA under LSR after2 hours (36 mg, P=0.0011; 72 mg, P<0.0001) and 5 hours (72 mg, P=0.0057), and under HSR after 2 and 5 hours (72 mg, P<0.05). Compared with ASA alone, CBT was markedly prolonged by clopidogrel plus ASA (ratio 6.4; P<0.0001) but only slightly by ximelagatran plus ASA (72 mg ximelagatran,ratio 1.4;P=0.0010).Both drug combinations were well tolerated. Oral ximelagatran plus ASA has a greater antithrombotic effect in this human ex vivo thrombosis model and a less prounounced prolongation of bleeding time than clopidogrel plus ASA.

Keywords

Clinical trials - oral anticoagulants - coagulation inhibitors - thrombin
 

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