Abstract
Summary. In recent years, the choice of recombinant factor VIII products, including those for subcutaneous administration, has expanded significantly. However, in the treatment of patients with hemophilia A, a number of unresolved issues remain, primarily those related to the treatment burden for patients and their relatives, insufficient bleeding control, and progression of musculoskeletal damage. We present
a clinical case of a 38-year-old patient with severe hemophilia A, hemophilic arthropathy of the ankle and knee joints who was switched from plasma-derived FVIII product to a recombinant single-chain FVIII (lonoctocog alfa). The therapeutic modification resulted in an increased residual FVIII activity and demonstrated clinical effectiveness. No adverse events were observed during treatment. This case illustrates the high efficacy and safety of recombinant single-chain FVIII (lonoctocog alfa) for bleeding prophylaxis in a patient with hemophilia A in real world clinical practice in Russia.
For citation: Andreeva T.A., ZalepukhininaO.E., KrasheninnikovaO.A., PozdnyakovaV.A., PetrovV.Yu. Clinical experience with lonoctocog alfa for prophylaxis in a patient with hemophilia A. Tromboz, gemostaz i reologiya. 2025;(2):129–134. (In Russ.).
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