Continuous Infusion of Turoctocog Alfa in Patients With Mild to Moderate Hemophilia A: A Case Series
- PMID: 38990524
- DOI: 10.1097/MJT.0000000000001713
Continuous Infusion of Turoctocog Alfa in Patients With Mild to Moderate Hemophilia A: A Case Series
Conflict of interest statement
M. Wayman, L. Nguyen, D. C. Moore, and M. A. Knovich: These authors have no conflicts of interest to declare. J. Arnall has been a member of a CTI BioPharma and HEMA Pharmaceutical Advisory Board and previously spoke for the Novo Nordisk (Hemophilia) Speaker's Bureau.
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- Srivastava A, Brewer AK, Mauser-Bunschoten EP, et al. Guidelines for the management of hemophilia. Haemophilia. 2013;19:e1–e47.
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- NovoEight [package Insert]. Plainsboro, NJ; Novo Nordisk Inc; 2018.
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- Takeyama M, Nogami K, Kobayashi R, et al. Continuous infusions of B domain-truncated recombinant factor VIII, turoctocog alfa, for orthopedic surgery in severe hemophilia A: first case report. Int J Hematol. 2018;108:199–202.
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- Takeyama M, Nøhr AM, Pollard D. Stability of turoctocog alfa, a recombinant factor VIII product, during continuous infusion in vitro. TH Open. 2020;4:e354–e361.
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- Lentz SR, Misgav M, Ozelo M, et al. Results from a large multinational clinical trial (guardian™1) using prophylactic treatment with turoctocog alfa in adolescent and adult patients with severe haemophilia A: safety and efficacy. Haemophilia. 2013;19:691–697.
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