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Half‐life extended factor VIII for the treatment of hemophilia A

Journal of thrombosis and haemostasis, 2015-06, Vol.13 (S1), p.S176-S179

Tiede, A.

2015

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Thromboembolic Risks of Non-Factor Replacement Therapies in Hemophilia

Hamostaseologie, 2017-01, Vol.37 (4), p.307

Tiede, A

2017

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Enhancing the pharmacokinetic properties of recombinant factor VIII: first‐in‐human trial of glycoPEGylated recombinant factor VIII in patients with hemophilia A

Journal of thrombosis and haemostasis, 2013-04, Vol.11 (4), p.670-678

2013

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Diagnostic and prognostic value of factor VIII binding antibodies in acquired hemophilia A: data from the GTH‐AH 01/2010 study

Journal of thrombosis and haemostasis, 2016-05, Vol.14 (5), p.940-947

2016

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Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single‐centre cohort study

Journal of thrombosis and haemostasis, 2008-04, Vol.6 (4), p.569-576

2008

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PK‐guided personalized prophylaxis with Nuwiq® (human‐cl rhFVIII) in adults with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-09, Vol.23 (5), p.697-704

2017

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QUANTITATIVE PHARMACOKINETIC MODEL TO CHARACTERIZE AND EXTRAPOLATE LONG-TERM FVIII ACTIVITY LEVELS IN PATIENTS WITH SEVERE HEMOPHILIA A TREATED WITH VALACTOCOGENE ROXAPARVOVEC

Hematology, Transfusion and Cell Therapy, 2023-10, Vol.45, p.S451

2023

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Prophylaxis vs. on-demand treatment with Nuwiq® (Human-cl rhFVIII) in adults with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-05, Vol.22 (3), p.374-380

2016

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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 : the official journal of the World Federation of Hemophilia, 2013-09, Vol.19 (5), p.691-697

2013

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Pharmacokinetics of a novel extended half‐life glycoPEGylated factor IX, nonacog beta pegol (N9‐GP) in previously treated patients with haemophilia B: results from two phase 3 clinical trials

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-07, Vol.23 (4), p.547-555

2017

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Anti‐FcγRIIB (CD32) Antibodies Differentially Modulate Murine FVIII‐Specific Recall Response in vitro

Scandinavian journal of immunology, 2017-08, Vol.86 (2), p.91-99

2017

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Management of acquired haemophilia A

Hamostaseologie, 2015, Vol.35 (4), p.311-318

2015

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A Comprehensive Analysis of the Cellular and EBV‐Specific MicroRNAome in Primary CNS PTLD Identifies Different Patterns Among EBV‐Associated Tumors

American journal of transplantation, 2014-11, Vol.14 (11), p.2577-2587

2014

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The first recombinant FVIII produced in human cells - an update on its clinical development programme

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (s1), p.1-9

2014

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siRNA Mediated Knockdown of Tissue Factor Expression in Pigs for Xenotransplantation

American journal of transplantation, 2015-05, Vol.15 (5), p.1407-1414

2015

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Co‐morbidities and bleeding in elderly patients with haemophilia—A survey of the German, Austrian and Swiss Society of Thrombosis and Haemostasis Research (GTH)

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-09, Vol.23 (5), p.721-727

2017

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Turoctocog alfa (recombinant factor VIII). Manufacturing, characteristics and clinical trial results

Hämostaseologie, 2015, Vol.35 (4), p.364-371

2015

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Bioequivalence between two serum-free recombinant factor VIII preparations (N8 and ADVATE®) - an open-label, sequential dosing pharmacokinetic study in patients with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-11, Vol.17 (6), p.854-859

2011

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Pain therapy in haemophilia in Germany. Patient survey (BESTH study)

Hämostaseologie, 2015, Vol.35 (2), p.167-173

2015

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Pharmacokinetics, phenotype and product choice in haemophilia B: how to strike a balance?

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-11, Vol.20 (s7), p.1-11

2014

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Interim results from a large multinational extension trial (guardian(™) 2) using turoctocog alfa for prophylaxis and treatment of bleeding in patients with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.e445-e449

2016

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Spotlight on the human factor: building a foundation for the future of haemophilia A management: report from a symposium on human recombinant FVIII at the World Federation of Hemophilia World Congress, Melbourne, Australia on 12 May 2014

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-01, Vol.21 Suppl 1 (s1), p.1-12

2015

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Risk of bleeding and haemorrhagic complication with rivaroxaban--periprocedural management of haemostasis

Hämostaseologie, 2012, Vol.32 (4), p.287

2012

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Increased amounts of von Willebrand factor are bound to microparticles after infusion of desmopressin

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-03, Vol.19 (2), p.236-241

2013

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Treatment of lupus-prone NZB/NZW F1 mice with recombinant soluble Fcγ receptor II (CD32)

Annals of the rheumatic diseases, 2008-02, Vol.67 (2), p.154-161

2008

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Half‐life extended factor VIII for the treatment of hemophilia A

Thromboembolic Risks of Non-Factor Replacement Therapies in Hemophilia

Enhancing the pharmacokinetic properties of recombinant factor VIII: first‐in‐human trial of glycoPEGylated recombinant factor VIII in patients with hemophilia A

Diagnostic and prognostic value of factor VIII binding antibodies in acquired hemophilia A: data from the GTH‐AH 01/2010 study

Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single‐centre cohort study

PK‐guided personalized prophylaxis with Nuwiq® (human‐cl rhFVIII) in adults with severe haemophilia A

QUANTITATIVE PHARMACOKINETIC MODEL TO CHARACTERIZE AND EXTRAPOLATE LONG-TERM FVIII ACTIVITY LEVELS IN PATIENTS WITH SEVERE HEMOPHILIA A TREATED WITH VALACTOCOGENE ROXAPARVOVEC

Prophylaxis vs. on-demand treatment with Nuwiq® (Human-cl rhFVIII) in adults with severe haemophilia A

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

Pharmacokinetics of a novel extended half‐life glycoPEGylated factor IX, nonacog beta pegol (N9‐GP) in previously treated patients with haemophilia B: results from two phase 3 clinical trials

Anti‐FcγRIIB (CD32) Antibodies Differentially Modulate Murine FVIII‐Specific Recall Response in vitro

Management of acquired haemophilia A

A Comprehensive Analysis of the Cellular and EBV‐Specific MicroRNAome in Primary CNS PTLD Identifies Different Patterns Among EBV‐Associated Tumors

The first recombinant FVIII produced in human cells - an update on its clinical development programme

siRNA Mediated Knockdown of Tissue Factor Expression in Pigs for Xenotransplantation

Co‐morbidities and bleeding in elderly patients with haemophilia—A survey of the German, Austrian and Swiss Society of Thrombosis and Haemostasis Research (GTH)

Turoctocog alfa (recombinant factor VIII). Manufacturing, characteristics and clinical trial results

Bioequivalence between two serum-free recombinant factor VIII preparations (N8 and ADVATE®) - an open-label, sequential dosing pharmacokinetic study in patients with severe haemophilia A

Pain therapy in haemophilia in Germany. Patient survey (BESTH study)

Pharmacokinetics, phenotype and product choice in haemophilia B: how to strike a balance?

Interim results from a large multinational extension trial (guardian(™) 2) using turoctocog alfa for prophylaxis and treatment of bleeding in patients with severe haemophilia A

Spotlight on the human factor: building a foundation for the future of haemophilia A management: report from a symposium on human recombinant FVIII at the World Federation of Hemophilia World Congress, Melbourne, Australia on 12 May 2014

Risk of bleeding and haemorrhagic complication with rivaroxaban--periprocedural management of haemostasis

Increased amounts of von Willebrand factor are bound to microparticles after infusion of desmopressin

Treatment of lupus-prone NZB/NZW F1 mice with recombinant soluble Fcγ receptor II (CD32)

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