Turoctocog alfa pegol (N8‐GP) in severe hemophilia A: Long‐term safety and efficacy in previously treated patients of all ages in the pathfinder8 study
Author:
Funder
Novo Nordisk
Publisher
Elsevier BV
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/rth2.12674
Reference27 articles.
1. WFH guidelines for the management of hemophilia;Srivastava;Haemophilia,2020
2. Extended half‐life recombinant products in haemophilia clinical practice ‐ expectations, opportunities and challenges;Chowdary;Thromb Res,2020
3. Enhancing the pharmacokinetic properties of recombinant factor VIII: first‐in‐human trial of glycoPEGylated recombinant factor VIII in patients with hemophilia A;Tiede;J Thromb Haemost,2013
4. N8‐GP: a new extended half‐life recombinant factor VIII product for hemophilia A;Chowdary;J Thromb Haemost,2020
5. An overview of the pathfinder clinical trials program: long‐term efficacy and safety of N8‐GP in patients with hemophilia A;Matsushita;J Thromb Haemost,2020
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2. Noninterventional study assessing joint health in persons with hemophilia A after switching to turoctocog alfa pegol: design of pathfinderReal;Research and Practice in Thrombosis and Haemostasis;2024-02
3. Long-term efmoroctocog alfa prophylaxis improves perceived pain, mental, and physical health in patients with hemophilia A: post hoc analysis of phase III trials using patient-reported outcomes;Therapeutic Advances in Hematology;2024-01
4. The immunogenicity, safety, and efficacy of N8-GP in previously untreated patients with severe hemophilia A: pathfinder6 end-of-trial results;Journal of Thrombosis and Haemostasis;2023-11
5. Real-World Experience of People with Hemophilia A Receiving Turoctocog Alfa Pegol (N8-GP): Results from a Patient Experience Survey;Patient Preference and Adherence;2023-11
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