Key result
Ximelagatran was noninferior to adjusted-dose warfarin for preventing stroke and systemic embolism in patients with nonvalvular atrial fibrillation.
Why the study?
Does oral ximelagatran prevent stroke and systemic embolism at least as effectively as adjusted-dose warfarin in patients with nonvalvular atrial fibrillation?
RCT
Open-label
Randomized
Yes
Does oral ximelagatran prevent stroke and systemic embolism at least as effectively as adjusted-dose warfarin in patients with nonvalvular atrial fibrillation?
Ximelagatran, an oral direct thrombin inhibitor, demonstrated noninferiority to warfarin for stroke prevention in atrial fibrillation in the SPORTIF III trial.
Answers are grounded in this paper and cite their sources.
Ximelagatran may simplify anticoagulation without INR monitoring in nonvalvular AF; leaves open safety, durability, and adoption from limited evidence synthesis.
The oral direct thrombin inhibitor ximelagatran (Exanta, AstraZeneca) is rapidly absorbed, is efficiently bioconverted to the active form, melagatran (AstraZeneca) and has shown efficacy and relative safety as an anticoagulant for prophylaxis and therapy of thromboembolism. Two Phase III trials, Stroke Prevention using an ORal Thrombin Inhibitor in atrial Fibrillation (SPORTIF V), have tested the hypothesis that oral ximelagatran, administered 36 mg twice daily without coagulation monitoring or dose adjustment, prevents stroke and systemic embolism at least as effectively as adjusted-dose warfarin (international normalized ratio, 2.0-3.0) in patients with nonvalvular atrial fibrillation. Both were randomized, multicenter trials (n > 3000 per trial) with blinded end-point assessment. The open-label SPORTIF III trial confirmed the noninferiority of ximelagatran versus warfarin. Publication of the full results from SPORTIF V is pending.
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Jonathan L. Halperin (2004) conducted an RCT in Nonvalvular atrial fibrillation. Ximelagatran vs. Adjusted-dose warfarin (INR 2.0-3.0) was evaluated on Stroke and systemic embolism. Ximelagatran was noninferior to adjusted-dose warfarin for preventing stroke and systemic embolism in patients with nonvalvular atrial fibrillation.
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