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AB0451 Rivaroxaban versus warfarin as secondary thromboprophylaxis in patients with antiphospholipid syndrome protocol: a randomized, multicentre, open-label, clinical trial
  1. J Cortés-Hernández1,
  2. L Saez-Comet2,
  3. M Perez-Conesa2,
  4. A Riera Mestre3,
  5. A Castro-Salomo4,
  6. S Parra4,
  7. J Cuquet-Pedragosa5,
  8. V Ortiz-Santamaria6,
  9. M Mauri-Plana7,
  10. P Suñe8,
  11. J Ordi-Ros9
  1. 1Vall Hebron Institute Research (Vhir), Barcelona
  2. 2Autoimmune Unit. Internal Medicine Department, Miguel Servet Hospital, Zaragoza
  3. 3VTE Unit. Internal Medicine Department, Bellvitge University Hospital, Barcelona
  4. 4Internal Medicine Department, Sant Joan de Reus University Hospital, Reus
  5. 5Internal Medicine Department
  6. 6Rheumatology Unit, Granollers University Hospital, Granollers
  7. 7Internal Medicine Department., Matarό Hospital, Matarό
  8. 8Pharmacy Department, Vall d'Hebron Hospital
  9. 9Autoimmune Unit. Internal Medicine Department, Vall Hebron Institute Research (Vhir), Barcelona, Spain


Background Long-term anticoagulation is widely used for secondary thromboprophylaxis in the antiphospholipid syndrome (APS) due to the high risk of recurrent events. Currently anticoagulation with vitamin K antagonists (VKAs) is the standard of care but have unpredictable pharmacodynamic properties that requiere monitoring for dose adjustment. Rivaroxaban, an orally active direct factor Xa inhibitor, has been shown to be effective and safe compared with warfarin for the treatment of venous thromboembolism and non valvular atrial fibrillation in major RCTs. No studies had been published in APS.

Objectives To investigate the efficacy and safety of rivaroxaban in preventing recurrent thrombosis in patients with APS compared with warfarin.

Methods This is a phase 3 randomized, multicenter, non-inferiority open-label RCT. 190 eligible APS patients with arterial or venous thrombotic history receiving warfarin will be stratified according the presence of SLE and venous/arterial thrombotic history and randomized (1:1) either to continue warfarin (standard of care, normalized ratio (INR) 2–3 or 2.5 to 3.5 in those with recurrent thrombotic episodes) or to switch to rivaroxaban (20 mg/day). The primary efficacy outcome is the development of any thrombotic event during the study period. Secondary efficacy outcomes include time to thrombosis, type of thrombosis (arterial or venous), overall causes of death, evaluation of a prognostic biomarker panel of recurrent thrombosis. The primary safety outcome will be major bleeding. Secondary safety outcomes include any adverse event and minor bleeding. The study has 3 years follow-up. First patient was included in March 2013 (EUDRA-CT:2010–019764–36).

Conclusions If the study demonstrates a non-inferior anticoagulant effect compared with warfarin, this would provide sufficient supporting evidence to make rivaroxaban a standard of care for the treatment of patients with APS with previous thrombotic history.

Disclosure of Interest None declared

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