Bayer gets European approval for Xarelto
Germany's Bayer Healthcare has been granted European marketing approval for its once-daily anticoagulant Xarelto (rivaroxaban) for the prevention of venous blood clots in adult patients undergoing elective hip or knee replacement surgery. The approval is based on a review of the data for the extensive RECORD clinical program involving almost 10,000 patients across three Phase III trials comparing the drug to market leader Sanofi-Aventis' Lovenox (enoxaparin). Bayer says it will begin the product's launch in European Union member states "very soon."
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