Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2017 Mar;28(2):152-162.
doi: 10.1097/MBC.0000000000000568.

Pharmacokinetics, efficacy, and safety of a plasma-derived VWF/FVIII concentrate (VONCENTO) for on-demand and prophylactic treatment in patients with von Willebrand disease (SWIFT-VWD study)

Affiliations
Multicenter Study

Pharmacokinetics, efficacy, and safety of a plasma-derived VWF/FVIII concentrate (VONCENTO) for on-demand and prophylactic treatment in patients with von Willebrand disease (SWIFT-VWD study)

Toshko J Lissitchkov et al. Blood Coagul Fibrinolysis. 2017 Mar.

Abstract

VONCENTO (CSL Behring Gmbh, Marburg, Germany) is a plasma-derived, high concentration, lower volume [relative to HAEMATE P (CSL Behring)], high-purity von Willebrand factor (VWF)/factor VIII (FVIII) concentrate with a VWF/FVIII ratio similar to HAEMATE P. This open-label, multicentre study investigated the pharmacokinetic, haemostatic efficacy, and safety profiles of VONCENTO in study participants at least 12 years of age with von Willebrand disease (VWD) who required treatment of nonsurgical bleeding (NSB) events or underwent surgery or prophylaxis. The first 12-month on-demand treatment period comprised a pharmacokinetic investigation and an efficacy analysis. After 12 months, qualifying study participants were switched to prophylactic therapy and included in a further 12-month efficacy analysis. In total, 21 study participants (including three adolescents, and 13 study participants with VWD type 3) received VONCENTO as on-demand treatment for 12 months. 'Excellent'/'good' haemostatic efficacy was achieved in 98.3% of the 407 NSB events assessed by investigators. Following the switch to prophylactic treatment, the total number of NSBs in eight patients markedly decreased from 304 to 10 (with haemostatic efficacy judged to be 'excellent' for all). The annualised bleeding rate also significantly decreased from a median of 26.5 events to one event. Safety assessments showed no inhibitory antibodies to either FVIII or VWF, no transmission of infectious agents, no thromboembolic events and no treatment-related serious adverse events. VONCENTO was shown to be well tolerated and provided excellent haemostatic efficacy in the treatment of bleeds or during prophylaxis in study participants with VWD, including also those with type 3, the severest form of VWD.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Study participant disposition. aFor PK study participants with type 3 von Willebrand disease only. PK, pharmacokinetics.
Fig. 2
Fig. 2
von Willebrand factor multimer comparison: VONCENTO and NHP. Image kindly provided by Professor Ulrich Budde. HMW, high molecular weight; IMW, intermediate molecular weight; LMW, low molecular weight; NHP, normal human plasma.

Similar articles

Cited by

References

    1. US Department of Health and Human Services, National Institute of Health. The Diagnosis, Evaluation and Management of von Willebrand Disease. National Heart Lung and Blood Institute. NIH Publication No. 08–5832. December 2007.
    1. Vischer UM, de Moerloose P. von Willebrand factor: from cell biology to the clinical management of von Willebrand's disease. Crit Rev Oncol Hematol 1999; 30:93–109. - PubMed
    1. Mannucci PM. Treatment of von Willebrand's disease. N Engl J Med 2004; 351:683–694. - PubMed
    1. Federici AB, Mannucci PM. Diagnosis and management of von Willebrand disease. Haemophilia 1999; 5 Suppl 2:28–37. - PubMed
    1. Mannucci PM, Ruggeri ZM, Pareti FI, Capitanio A. 1-Deamino-8-d-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands’ diseases. Lancet 1977; 1:869–872. - PubMed

Publication types