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2. Efficacy and safety of BAY 81-8973, a full-length recombinant factor VIII: results from the LEOPOLD I trial. Saxena K; Lalezari S; Oldenburg J; Tseneklidou-Stoeter D; Beckmann H; Yoon M; Maas Enriquez M Haemophilia; 2016 Sep; 22(5):706-12. PubMed ID: 27339736 [TBL] [Abstract][Full Text] [Related]
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4. Efficacy and safety of prophylaxis with BAY 81-8973 in Chinese patients with severe haemophilia A enrolled in the LEOPOLD II trial. Yang R; Sun J; Zhao Y; Wang X; Wu D; Tseneklidou-Stoeter D; Wu J; Church N Haemophilia; 2019 May; 25(3):e153-e158. PubMed ID: 30993836 [TBL] [Abstract][Full Text] [Related]
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9. Canadian clinical experience on switching from standard half-life recombinant factor VIII (rFVIII), octocog alfa, to extended half-life rFVIII, damoctocog alfa pegol, in persons with haemophilia A ≥ 12 years followed in a Comprehensive Hemophilia Care Program in Canada. Matino D; Germini F; Chan AKC; Decker K; Iserman E; Chelle P; Edginton AN; Oladoyinbo O; Trinari E; Keepanasseril A; Iorio A Haemophilia; 2024 Mar; 30(2):345-354. PubMed ID: 38379181 [TBL] [Abstract][Full Text] [Related]
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11. Pharmacokinetic properties of BAY 81-8973, a full-length recombinant factor VIII. Shah A; Delesen H; Garger S; Lalezari S Haemophilia; 2015 Nov; 21(6):766-71. PubMed ID: 25952661 [TBL] [Abstract][Full Text] [Related]
12. Analysis of the Japanese subgroup in LEOPOLD II: a phase 2/3 study of BAY 81-8973, a new recombinant factor VIII product. Fujii T; Hanabusa H; Shima M; Morinaga T; Fukutake K Int J Hematol; 2017 Mar; 105(3):280-286. PubMed ID: 27832514 [TBL] [Abstract][Full Text] [Related]
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20. Pharmacokinetics, prophylactic effects, and safety of a new recombinant FVIII formulated with sucrose (BAY 14-2222) in Japanese patients with hemophilia A. Shirahata A; Fukutake K; Takamatsu J; Shima M; Yoshioka A Int J Hematol; 2000 Jul; 72(1):101-7. PubMed ID: 10979218 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]