Clinical experience with moroctocog alfa (AF-CC) in younger paediatric patients with severe haemophilia A: Two open-label studies

Author:

Rusen L.1,Kavakli K.2ORCID,Korth-Bradley J.3ORCID,Huard F.4,Rendo P.3,Fuiman J.3,Baumann J. A.3,Smith L.3,Alvey C.5,Rupon J.3ORCID

Affiliation:

1. Prof. Dr. C. T. Nicolau National Institute for Transfusional Haematology; Bucharest Romania

2. Department of Haematology; Ege University Children's Hospital; Izmir Turkey

3. Global Product Development; Pfizer Inc.; Collegeville PA USA

4. Global Product Development; Pfizer Inc.; Paris France

5. Pfizer Inc.; Groton CT USA

Funder

Pfizer

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference19 articles.

1. An improved manufacturing process for Xyntha/ReFacto AF;Kelley;Haemophilia,2010

2. Clinical evaluation of moroctocog alfa (AF-CC), a new generation of B-domain deleted recombinant factor VIII (BDDrFVIII) for treatment of haemophilia A: demonstration of safety, efficacy, and pharmacokinetic equivalence to full-length recombinant factor VIII;Recht;Haemophilia,2009

3. Xyntha [package insert] Philadelphia, PA Wyeth Pharmaceuticals (Pfizer Inc) 2015

4. European Medicines Agency Summary of Product Characteristics: ReFacto AF http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Product_Information/human/000232/WC500049008.pdf

5. Prospective surveillance study of haemophilia A patients switching from moroctocog alfa or other factor VIII products to moroctocog alfa albumin-free cell culture (AF-CC) in usual care settings;Parra Lopez;Thromb Haemost,2015

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