Literature DB >> 18416588

Sucrose-formulated octocog alfa: a review of its use in patients with haemophilia A.

James E Frampton1, Antona J Wagstaff.   

Abstract

Sucrose-formulated octocog alfa (Kogenate Bayer, Kogenate FS, Helixate FS, Helixate nexgen) is a full-length recombinant human coagulation factor VIII (FVIII) product that is purified and formulated without the addition of human serum albumin and is stabilized with sucrose. The purification process of this formulation includes a solvent/detergent viral inactivation step. Sucrose-formulated octocog alfa is approved in the EU and US for the treatment of bleeding in patients with haemophilia A (congenital FVIII deficiency). Additionally, it is approved in the EU for the prophylaxis of bleeding in patients with haemophilia A and as a continuous infusion treatment in patients undergoing major surgery. Sucrose-formulated octocog alfa is effective and well tolerated as a FVIII replacement therapy in patients with haemophilia A, including those with severe disease undergoing major surgery. The therapeutic profile of this sucrose-formulated product cannot be compared with that of other octocog alfa or moroctocog alfa products because of a lack of head-to-head comparative studies. Pathogen transmission has not been reported with use of sucrose-formulated octocog alfa. Available data indicate that sucrose-formulated octocog alfa is an appropriate alternative to other recombinant FVIII products for the treatment and prophylaxis of bleeding episodes in adults and children with haemophilia A.

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Year:  2008        PMID: 18416588     DOI: 10.2165/00003495-200868060-00007

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  53 in total

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Journal:  Transfusion       Date:  2002-11       Impact factor: 3.157

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Authors:  K Peerlinck; C Hermans
Journal:  Haemophilia       Date:  2006-11       Impact factor: 4.287

9.  IgG formation to mammalian proteins in hemophilia A patients following treatment with a new recombinant human factor VIII.

Authors:  P Larson; C Zhang; E Gorina; E Burmeister Getz
Journal:  J Thromb Haemost       Date:  2004-06       Impact factor: 5.824

Review 10.  Immune tolerance therapy for factor VIII inhibitors: moving from empiricism to an evidence-based approach.

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Journal:  J Thromb Haemost       Date:  2007-07       Impact factor: 5.824

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