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Klukowska A, Skotnicki A, Lissitchkov TJ et al. Efficacy, safety and pharmacokinetic results of a phase II/III, multicentre, double-blinded, randomized, cross-over study with a plasma-derived von Willebrand Factor/factor VIII concentrate (Voncento (R)) in subjects with hemophilia A (the SWIFT-HA study). F1000Posters 2015, 6:214 (poster)

Efficacy, safety and pharmacokinetic results of a phase II/III, multicentre, double-blinded, randomized, cross-over study with a plasma-derived von Willebrand Factor/factor VIII concentrate (Voncento ®) in subjects with hemophilia A (the SWIFT-HA study)

A Klukowska, A Skotnicki, T J Lissitchkov, V Mamonov, E Buevich, K Kuliczkowski, S Goranov, J Kloczko, S Stankovic, L Gercheva, T Chernova, A Hellmann, A Dmoszynska, K Zawilska, C Joch1, W Seifert
Published 18 Mar 2015
Author Affiliations
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Published 18 Mar 2015

Efficacy, safety and pharmacokinetic results of a phase II/III, multicentre, double-blinded, randomized, cross-over study with a plasma-derived von Willebrand Factor/factor VIII concentrate (Voncento ®) in subjects with hemophilia A (the SWIFT-HA study)

[version 1; not peer reviewed]

A Klukowska, A Skotnicki, T J Lissitchkov, V Mamonov, E Buevich, K Kuliczkowski, S Goranov, J Kloczko, S Stankovic, L Gercheva, T Chernova, A Hellmann, A Dmoszynska, K Zawilska, C Joch1, W Seifert
Author Affiliations
1 Department of Clinical Research and Development, CSL Behring, GmBH, Germany
Presented at
World Federation of Hemophilia (WFH) World Congress 2014
Abstract
Competing Interests

C Joch and W Seifert are CSL Behring employees.

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