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Antihemophilic Factor, Human Recombinant 1 UNT Injection [Kovaltry]

Known as: Kovaltry 1 UNT Injection, ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT 3000 [iU] in 5 mL INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [Kovaltry], ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT 2000 [iU] in 5 mL INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [Kovaltry] 
National Institutes of Health

Papers overview

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2020
2020
To report interim data from TAURUS, a study assessing real‐world prophylactic treatment with unmodified, full‐length recombinant… 
2020
2020
BAY 81‐8973 (Kovaltry®), a full‐length, unmodified, recombinant human factor VIII, provided excellent bleeding control for… 
2019
2019
BAY 81‐8973 (Kovaltry®) is a full‐length, unmodified recombinant human factor VIII approved in China for prophylaxis and on… 
Review
2019
Review
2019
The current interest in recombinant factor VIII (rFVIII) products stems from the fact that they offer a technological solution to… 
Review
2018
Review
2018
BAY 81-8973 (Kovaltry®) is an unmodified, full-length recombinant factor VIII (rFVIII) approved for the prevention and treatment… 
Review
2018
Review
2018
Background: BAY 81-8973 (Kovaltry®, Bayer) is an unmodified full-length recombinant FVIII launched in 2016 in Europe and the US… 
2017
2017
Farmeconomia. Health economics and therapeutic pathways 2017; 18(1) © SEEd All rights reserved Dal punto di vista economico, il… 
Review
2016
Review
2016
BAY 81-8973 (octocog alfa; Kovaltry®) is an unmodified, full-length, recombinant factor VIII (FVIII) concentrate with the same… 
2016
2016
vazioni della World Federation of Hemophilia riportando una prevalenza della malattia di 6,2/100.000 abitanti; nel 2013, dei 3…