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Efficacy and safety of fitusiran prophylaxis in people with haemophilia A or haemophilia B with inhibitors (ATLAS-INH): a multicentre, open-label, randomised phase 3 trial

The Lancet (British edition), 2023-04, Vol.401 (10386), p.1427-1437

2023

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S303: A PHASE 3 STUDY (ATLAS‐PPX) TO EVALUATE EFFICACY AND SAFETY OF FITUSIRAN IN PEOPLE WITH HAEMOPHILIA A OR B WHO HAVE SWITCHED FROM PRIOR CLOTTING FACTOR CONCENTRATE OR BYPASSING AGENT PROPHYLAXIS

HemaSphere, 2023-08, Vol.7 (S3), p.e643526e-n/a

2023

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Long‐term safety and efficacy of N8‐GP in previously treated adults and adolescents with hemophilia A: Final results from pathfinder2

Journal of thrombosis and haemostasis, 2020-09, Vol.18 (S1), p.5-14

2020

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Fitusiran prophylaxis in people with hemophilia A or B who switched from prior BPA/CFC prophylaxis: the ATLAS-PPX trial

Blood, 2024-05, Vol.143 (22), p.2256-2269

2024

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Phase 3 Trial of Concizumab in Hemophilia with Inhibitors

The New England journal of medicine, 2023-08, Vol.389 (9), p.783-794

2023

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Fitusiran prophylaxis in people with severe haemophilia A or haemophilia B without inhibitors (ATLAS-A/B): a multicentre, open-label, randomised, phase 3 trial

The Lancet. Haematology, 2023-05, Vol.10 (5), p.e322-e332

2023

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Safety, pharmacokinetics, and pharmacodynamics of a next‐generation subcutaneously administered coagulation factor IX variant, dalcinonacog alfa, in previously treated hemophilia B patients

Journal of thrombosis and haemostasis, 2021-04, Vol.19 (4), p.967-975

2021

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The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A

Blood Research, 2019, 54(3), , pp.204-209

2019

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Clinical Analysis of Hospitalized Patients with Hemophilia A: Single-hemophilia Treatment Center Experience in Korea over 10 years

Blood Research, 2021, 56(3), , pp.141-149

2021

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Clinical data on treatment regimen and use of medication among patients with hemophilia B in Korea

Blood Research, 2024, 59(3), , pp.27-27

2024

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Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array

Haematologica (Roma), 2012-02, Vol.97 (2), p.304-309

2012

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Mutation analysis of factor VIII in Korean patients with severe hemophilia A

International journal of hematology, 2010-06, Vol.91 (5), p.784-791

2010

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Subgroup analysis of a phase 2/3 study of rurioctocog alfa pegol in patients with severe hemophilia A: efficacy and safety in previously treated Korean patients

Blood Research, 2019, 54(3), , pp.198-203

2019

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A pediatric case of idiopathic Harlequin syndrome

Korean journal of pediatrics, 2016-11, Vol.59 (Suppl 1), p.S125

2016

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Effects of coagulation factor concentrate prophylaxis in moderate and severe hemophilia A patients at a single hemophilia center in Korea

Korean journal of pediatrics, 2013-07, Vol.56 (7), p.291

2013

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Effects of coagulation factor concentrate prophylaxis in moderate and severe hemophilia A patients at a single hemophilia center in Korea

Korean journal of pediatrics, 2013, Vol.56 (7), p.291-297

2013

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A pediatric case of idiopathic Harlequin syndrome

Korean journal of pediatrics, 2016, Vol.59 (1), p.125-128

2016

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Effects of thyroxine on hyperkalemia and renal cortical Na+, K+ - ATPase activity induced by cyclosporin A

Journal of Korean medical science, 2002-10, Vol.17 (5), p.625-632

2002

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Active Lifestyle in Patients with Hemophilia A or B with Inhibitors on Once-Daily Subcutaneous Concizumab Prophylaxis: Results from the Phase 3 explorer7 Study

Blood, 2022-11, Vol.140 (Supplement 1), p.5634-5636

2022

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Fitusiran, an Investigational siRNA Therapeutic Targeting Antithrombin for the Treatment of Hemophilia: First Results from a Phase 3 Study to Evaluate Efficacy and Safety in People with Hemophilia a or B without Inhibitors (ATLAS-A/B)

Blood, 2021-12, Vol.138 (Supplement 2), p.LBA-3-LBA-3

2021

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Clinical evaluation of glycoPEGylated recombinant FVIII: Efficacy and safety in severe haemophilia A

Thrombosis and haemostasis, 2017, Vol.117 (2), p.252-261

2017

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Reticulocyte hemoglobin content for the diagnosis of iron deficiency in young children with acute infection

Korean journal of pediatrics, 2008, Vol.51 (8), p.827

2008

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Phase 1/2 Trial of Subcutaneously Administered Factor IX Variant CB2679d/ISU304: Pharmacokinetics and Activity

Blood, 2017-12, Vol.130 (Suppl_1), p.87-87

2017

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Once-Weekly Prophylactic Treatment Versus on-Demand Treatment of Nonacog Alfa in Patients with Moderately Severe to Severe Hemophilia B

Blood, 2014-12, Vol.124 (21), p.1523-1523

2014

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The Value of Preoperative Coagulation Screening in Children Undergoing Surgery

Korean journal of hematology, 2008, Vol.43 (2), p.98

2008

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Efficacy and safety of fitusiran prophylaxis in people with haemophilia A or haemophilia B with inhibitors (ATLAS-INH): a multicentre, open-label, randomised phase 3 trial

S303: A PHASE 3 STUDY (ATLAS‐PPX) TO EVALUATE EFFICACY AND SAFETY OF FITUSIRAN IN PEOPLE WITH HAEMOPHILIA A OR B WHO HAVE SWITCHED FROM PRIOR CLOTTING FACTOR CONCENTRATE OR BYPASSING AGENT PROPHYLAXIS

Long‐term safety and efficacy of N8‐GP in previously treated adults and adolescents with hemophilia A: Final results from pathfinder2

Fitusiran prophylaxis in people with hemophilia A or B who switched from prior BPA/CFC prophylaxis: the ATLAS-PPX trial

Phase 3 Trial of Concizumab in Hemophilia with Inhibitors

Fitusiran prophylaxis in people with severe haemophilia A or haemophilia B without inhibitors (ATLAS-A/B): a multicentre, open-label, randomised, phase 3 trial

Safety, pharmacokinetics, and pharmacodynamics of a next‐generation subcutaneously administered coagulation factor IX variant, dalcinonacog alfa, in previously treated hemophilia B patients

The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A

Clinical Analysis of Hospitalized Patients with Hemophilia A: Single-hemophilia Treatment Center Experience in Korea over 10 years

Clinical data on treatment regimen and use of medication among patients with hemophilia B in Korea

Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array

Mutation analysis of factor VIII in Korean patients with severe hemophilia A

Subgroup analysis of a phase 2/3 study of rurioctocog alfa pegol in patients with severe hemophilia A: efficacy and safety in previously treated Korean patients

A pediatric case of idiopathic Harlequin syndrome

Effects of coagulation factor concentrate prophylaxis in moderate and severe hemophilia A patients at a single hemophilia center in Korea

Effects of coagulation factor concentrate prophylaxis in moderate and severe hemophilia A patients at a single hemophilia center in Korea

A pediatric case of idiopathic Harlequin syndrome

Effects of thyroxine on hyperkalemia and renal cortical Na+, K+ - ATPase activity induced by cyclosporin A

Active Lifestyle in Patients with Hemophilia A or B with Inhibitors on Once-Daily Subcutaneous Concizumab Prophylaxis: Results from the Phase 3 explorer7 Study

Fitusiran, an Investigational siRNA Therapeutic Targeting Antithrombin for the Treatment of Hemophilia: First Results from a Phase 3 Study to Evaluate Efficacy and Safety in People with Hemophilia a or B without Inhibitors (ATLAS-A/B)

Clinical evaluation of glycoPEGylated recombinant FVIII: Efficacy and safety in severe haemophilia A

Reticulocyte hemoglobin content for the diagnosis of iron deficiency in young children with acute infection

Phase 1/2 Trial of Subcutaneously Administered Factor IX Variant CB2679d/ISU304: Pharmacokinetics and Activity

Once-Weekly Prophylactic Treatment Versus on-Demand Treatment of Nonacog Alfa in Patients with Moderately Severe to Severe Hemophilia B

The Value of Preoperative Coagulation Screening in Children Undergoing Surgery

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