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Patients hospitalized with acute medical illnesses are at risk for venous thromboembolism (VTE), but whether the risk persists following discharge is uncertain. Now, investigators have conducted an industry-supported, phase III, multinational, randomized, double-blind trial in this setting to determine the safety and effectiveness of extended prophylaxis with betrixaban, a new oral anticoagulant that inhibits factor Xa, achieves a maximum concentration 3 to 4 hours after ingestion, and has a half-life of 19 to 25 hours.
A total of 7513 patients hospitalized with acute medical illnesses received either standard subcutaneous enoxaparin for 10±4 days followed by placebo for 35 to 42 days or placebo for 10±4 days followed by betrixaban for 35 to…