Revised terminal half‐life of nonacog alfa as derived from extended sampling data: A real‐world study involving 64 haemophilia B patients on nonacog alfa regular prophylaxis
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T. Lambert | A. Harroche | L. Ardillon | C. Berger | P. Chamouni | V. Gay | B. Tardy | S. Claeyssens | X. Delavenne | M. Trossaert | P. Chelle | A. Montmartin
[1] A. Iorio,et al. Terminal half‐life of FVIII and FIX according to age, blood group and concentrate type: Data from the WAPPS database , 2021, Journal of thrombosis and haemostasis : JTH.
[2] E. Santagostino,et al. WFH Guidelines for the Management of Hemophilia, 3rd edition , 2020, Haemophilia : the official journal of the World Federation of Hemophilia.
[3] A. Iorio,et al. Development and evaluation of the population pharmacokinetic models for FVIII and FIX concentrates of the WAPPS‐Hemo project , 2020, Haemophilia : the official journal of the World Federation of Hemophilia.
[4] A. Iorio,et al. Tailoring treatment of haemophilia B: accounting for the distribution and clearance of standard and extended half-life FIX concentrates , 2017, Thrombosis and Haemostasis.
[5] R. Labadie,et al. Confirmation of longer FIX activity half-life with prolonged sample collection after single doses of nonacog alfa in patients with haemophilia B , 2017, Thrombosis and Haemostasis.
[6] D. Stafford. Extravascular FIX and coagulation , 2016, Thrombosis Journal.
[7] J. Korth-Bradley,et al. Population pharmacokinetic modelling of factor IX activity after administration of recombinant factor IX in patients with haemophilia B , 2016, Haemophilia : the official journal of the World Federation of Hemophilia.
[8] K. Kuliczkowski,et al. Once‐weekly prophylactic treatment vs. on‐demand treatment with nonacog alfa in patients with moderately severe to severe haemophilia B , 2016, Haemophilia : the official journal of the World Federation of Hemophilia.
[9] J. Korth-Bradley,et al. Pharmacokinetics, Efficacy, and Safety of Nonacog Alfa in Previously Treated Patients with Moderately Severe to Severe Hemophilia B. , 2016, Clinical therapeutics.
[10] Hesham S. Al-Sallami,et al. Prediction of Fat-Free Mass in Children , 2015, Clinical Pharmacokinetics.
[11] L. Valentino,et al. Multicentre, randomized, open‐label study of on‐demand treatment with two prophylaxis regimens of recombinant coagulation factor IX in haemophilia B subjects , 2014, Haemophilia : the official journal of the World Federation of Hemophilia.
[12] J. Dumont,et al. Phase 3 study of recombinant factor IX Fc fusion protein in hemophilia B. , 2013, The New England journal of medicine.
[13] K. A. Stafford,et al. Evidence of clinically significant extravascular stores of factor IX , 2013, Journal of thrombosis and haemostasis : JTH.
[14] S. Björkman. Population pharmacokinetics of recombinant factor IX: implications for dose tailoring , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[15] T. Lissitchkov,et al. Head‐to‐head comparison of the pharmacokinetic profiles of a high‐purity factor IX concentrate (AlphaNine®) and a recombinant factor IX (BeneFIX®) in patients with severe haemophilia B , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[16] J. Mahlangu,et al. Guidelines for the management of hemophilia , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[17] P. Mannucci,et al. Pharmacokinetic properties of IB1001, an investigational recombinant factor IX, in patients with haemophilia B: repeat pharmacokinetic evaluation and sialylation analysis , 2012, Haemophilia : the official journal of the World Federation of Hemophilia.
[18] P. Monahan,et al. Abnormal hemostasis in a knock‐in mouse carrying a variant of factor IX with impaired binding to collagen type IV , 2009, Journal of thrombosis and haemostasis : JTH.
[19] L. Valentino,et al. Reformulated BeneFix®: efficacy and safety in previously treated patients with moderately severe to severe haemophilia B , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.