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New data support the safety and tolerability of the novel oral anticoagulant Exanta for stroke prevention in patients with atrial fibrillation

ients with atrial fibrillation.'

The longer-term phase II, SPORTIF IV, data in this important indication will be presented later this year. The phase III SPORTIF programme, comprising the SPORTIF III and V studies, is the largest-ever programme conducted in this indication with more than 6,200 patients enrolled.

Exanta is being investigated in a large clinical trials programme, including venous thromboembolism (VTE) prophylaxis in orthopaedic surgery, deep vein thrombosis (DVT) treatment, stroke prevention in atrial fibrillation and acute coronary syndrome. To date, more than 15,000 patients in 30 countries have been involved in clinical trials.


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Contact: Jonathan Wilson
jonathan.wilson@ketchum.com
44-7968-799-349
Ketchum
3-Sep-2001


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