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Published in 2022 at "Critical reviews in oncology/hematology"
DOI: 10.1016/j.critrevonc.2022.103678
Abstract: This review compares the methodology of published clinical studies investigating the extended-half-life (EHL) factor VIII (FVIII) products, rFVIIIFc (efmoroctocog alfa, Elocta®/Eloctate®), BAY 94-9027 (damoctocog alfa pegol, Jivi®), BAX 855 (rurioctocog alfa pegol, Adynovate®) and N8-GP… read more here.
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Published in 2017 at "Progress in Nuclear Energy"
DOI: 10.1016/j.pnucene.2017.07.010
Abstract: Abstract A new variational approach with anisotropic scattering kernel for first order neutron transport equation based on Finite Element Method (FEM) and Double- P N ( DP N ) approximation has been introduced. In presented… read more here.
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Published in 2024 at "Journal of Crohn's and Colitis"
DOI: 10.1093/ecco-jcc/jjad212.1041
Abstract: Tumor necrosis factor (TNF)-like ligand 1A (TL1A) mediates a broad spectrum of pro-inflammatory and fibrotic effects and is implicated in the pathogenesis of several immunologic disorders. Blockade of the interaction of TL1A with its cognate… read more here.
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Published in 2025 at "Journal of pediatric hematology/oncology"
DOI: 10.1097/mph.0000000000003101
Abstract: OBJECTIVE In recent years, one of the most significant advancements in hemophilia treatment has been the introduction of extended half-life (EHL) factors. This study aims to identify the 50 most influential articles on EHL factor… read more here.
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Published in 2017 at "Haemophilia"
DOI: 10.1111/hae.13191
Abstract: Nonacog beta pegol (N9‐GP) is a glycoPEGylated recombinant factor IX (FIX) with an extended half‐life developed for routine prophylaxis and the prevention and treatment of bleeding episodes in patients with haemophilia B. read more here.
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Published in 2017 at "Haemophilia"
DOI: 10.1111/hae.13246
Abstract: N8‐GP (turoctocog alfa pegol) is an extended half‐life glycoPEGylated recombinant factor VIII (FVIII) product developed for the prevention and treatment of bleeds in haemophilia A patients. read more here.
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Published in 2019 at "Haemophilia"
DOI: 10.1111/hae.13758
Abstract: Extended half‐life (EHL) factor VIII (FVIII) and IX (FIX) products are intended to decrease the burden of prophylaxis for patients with haemophilia A or B. Whether these newer concentrates have led to meaningful clinical practice… read more here.
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Published in 2019 at "Haemophilia"
DOI: 10.1111/hae.13834
Abstract: The concept of replacement therapy in haemophilia is changing significantly thanks to the switch from standard products to extended half‐life products. These novel drugs are showing beneficial effects overcoming current prophylaxis limitations by reducing the… read more here.
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Published in 2020 at "Haemophilia"
DOI: 10.1111/hae.13978
Abstract: The performance of surgery and invasive procedures in patients with haemophilia is currently facing new challenges globally. The first is the appropriate application of low‐dose protocols of clotting factor concentrates (CFC) achieving adequate perioperative haemostasis… read more here.
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Published in 2022 at "Haemophilia"
DOI: 10.1111/hae.14576
Abstract: Only few studies have presented results from real‐world clinical use of Extended Half‐Life (EHL) products in children with haemophilia (CWH). read more here.