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References

References: 1. Kovaltry Product Monograph, Bayer Inc., May 30, 2024. 2. Data on file 9, Bayer Inc., March 31, 2021. 3. Shah A, et al. Pharmacokinetic properties of BAY 81-8973, Bayer’s full-length recombinant factor VIII product. Haemophilia 2015;1–6. 4. Kavakli K, et al. Prophylaxis vs. on-demand treatment with BAY 81-8973, a full-length plasma protein-free recombinant factor VIII product: results from a randomized trial (LEOPOLD II). J Thromb Haemost 2015;13:360–9. 5. Ljung R, et al. BAY 81-8973 safety and efficacy for prophylaxis and treatment of bleeds in previously treated children with severe haemophilia A: results of the LEOPOLD Kids Trial. Haemophilia 2016;22(3):354–60. 6. World Federation of Hemophilia. Guidelines for the management of hemophilia. 2nd edition. Blackwell Publishing Ltd., 2012. 7. Iorio A, et al. Estimating and interpreting the pharmacokinetic profiles of individual patients with hemophilia A or B using a population pharmacokinetic approach: communication from the SSC of the ISTH. J Thromb Haemost 2017;15:2461–5. 8. Association of Hemophilia Clinic Directors of Canada (AHCDC), 2018. 9. Eloctate® Product Monograph, sanofi-aventis Canada Inc., September 25, 2020. 10. Nuwiq® Product Monograph, Octapharma Canada Inc., December 14, 2018. 11. Canadian Blood Services, Customer Letter, October 31, 2017.