Safety of recombinant activated factor VII (rFVIIa) in patients with congenital haemophilia with inhibitors: overall rFVIIa exposure and intervals following high (>240 μg kg−1) rFVIIa doses across clinical trials and registries

Author:

Shapiro A. D.1,Neufeld E. J.2,Blanchette V.3,Salaj P.4,Gut R. Z.5,Cooper D. L.5

Affiliation:

1. Indiana Hemophilia and Thrombosis Center; Indianapolis IN USA

2. Division of Hematology/Oncology; Boston Children's Hospital; Boston MA USA

3. Department of Pediatrics, Hospital for Sick Children; Toronto Canada

4. Institute of Hematology and Blood Transfusion; Prague Czech Republic

5. Clinical Development and Medical Affairs - Biopharm, Novo Nordisk Inc.; Plainsboro NJ USA

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

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