An open-label, multi-centre, post-marketing study to assess the efficacy and safety of a plasma-derived VWF/FVIII concentrate in patients with von Willebrand disease
Haemophilia
.
2024 Jan;30(1):236-240.
doi: 10.1111/hae.14868.
Epub 2023 Nov 29.
Authors
Wolfgang Miesbach
1
,
Susan Halimeh
2
,
Helen Platokouki
3
,
Maria Podolak-Dawidziak
4
,
Joanna Zdziarska
5
,
Bartosz Korczowski
6
,
Pratima Chowdary
7
,
Steve Austin
8
,
Carolyn Millar
9
,
Jayanthi Alamelu
10
,
Tobias Rogosch
11
,
Ingrid Pabinger
12
Affiliations
1
Haemophilia Centre, Medical Clinic II, Institute of Transfusion Medicine, Goethe University Hospital, Frankfurt am Main, Germany.
2
Coagulation Research Center, Duisburg, Germany.
3
"Aghia Sophia" Children's Hospital, Athens, Greece.
4
Department of Haematology, Blood Neoplasms and Bone Marrow Transplantation, Medical University of Wroclaw, Wroclaw, Poland.
5
Department of Haematology, University Hospital, Jagiellonian University Medical College, Cracow, Poland.
6
Department of Pediatrics, Institute of Medical Sciences, Medical College, University of Rzeszow, Rzeszow, Poland.
7
Katharine Dormandy Haemophilia and Thrombosis Centre, Royal Free Hospital, London, UK.
8
St George's Healthcare NHS Trust Haemophilia Centre, London, UK.
9
Imperial College, London, UK and Imperial College Healthcare NHS Trust, London, UK.
10
Children's Haemophilia Centre, Evelina London Children's Hospital, London, UK.
11
CSL Behring, Marburg, Germany.
12
Medical University of Vienna, Vienna, Austria.
PMID:
38030954
DOI:
10.1111/hae.14868
No abstract available
Publication types
Letter
MeSH terms
Factor VIII / adverse effects
Humans
Patients
von Willebrand Diseases* / drug therapy
von Willebrand Factor / therapeutic use
Substances
von Willebrand Factor
Factor VIII
Grants and funding
CSL Behring