Repeated short-interval administration of efanesoctocog alfa is not associated with increased global coagulation potential in hemophilia A mice
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Updated: May 31, 2026

Tail Vein Transection Bleeding Model in Fully Anesthetized Hemophilia A Mice
Published on: September 30, 2021
Yuki Kawasaki1, Yuto Nakajima2, Keiji Nogami1
1Department of Pediatrics, Nara Medical University, 840 Shijo-Cho, Kashihara, Nara, 634-8522, Japan.
Abstract:
Efanesoctocog alfa is an extended half-life recombinant factor VIII (FVIII) designed for prophylaxis in hemophilia A (HA). However, global coagulation potential after repeated short-interval dosing remains unclear. We assessed coagulation potential following repeated short-interval administration of efanesoctocog alfa. Efanesoctocog alfa and rurioctocog alfa (1, 2, and 3 IU/mL) were added to FVIII-deficient plasma samples, and coagulation potential was assessed using thrombin generation assays. Efanesoctocog alfa and rurioctocog alfa were intravenously administered at 100 IU/kg to HA mice once every 24 h for three consecutive days. Coagulation function was assessed by rotational thromboelastometry. Activated partial thromboplastin time (aPTT), FVIII activity by chromogenic assay (FVIII:C), thrombin-antithrombin complex (TAT), and D-dimer were measured 5 min after each dose. Thrombin generation potential in FVIII-deficient plasma spiked with efanesoctocog alfa was comparable to that in plasma spiked with rurioctocog alfa. In HA mice, rotational thromboelastometry parameters, aPTT, TAT, and D-dimer were similar with efanesoctocog alfa and rurioctocog alfa, whereas FVIII:C by chromogenic assay was higher with efanesoctocog alfa than with rurioctocog alfa. In conclusion, global coagulation potential after short-interval administration of efanesoctocog alfa was similar to that after rurioctocog alfa under the experimental conditions.
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