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XARELTO®

(rivaroxaban)

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XARELTO - Reversal Agents in Human Studies - Andexanet alfaa (PRT064445) - Phase 2 Study

Last updated : 05/16/2024

A phase 2 study in healthy subjects confirmed a dose-dependent decrease in anti–factor Xa activity and a return of anti–factor Xa activity to placebo levels approximately 2 hours after treatment.1

>10%

>10% of AEs were infusion-related reactions and postural dizziness.1

0

Thrombotic events and serious or severe AEs1

aAndexxa® (coagulation factor Xa [recombinant], inactivated-zhzo) is a product of AstraZeneca. Please refer to the Andexxa Prescribing Information for complete product information or call AstraZeneca at 1-800-236-9933.

AE, adverse event.

Reference

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1. Crowther M, Mathur V, Kitt M, et al. A phase 2, randomized, double-blind, placebo-controlled trial demonstrating reversal of rivaroxaban-induced anticoagulation in healthy subjects by andexanet alfa (PRT064445), an antidote for FXa inhibitors. Poster presented at: The 55th American Society of Hematology (ASH) Annual Meeting and Exposition; December 6-10, 2013; New Orleans, LA.