Literature DB >> 16392876

Octocog alfa, plasma/albumin-free method.

Paul L McCormack1, Greg L Plosker.   

Abstract

Octocog alfa, plasma/albumin-free method (octocog alfa-PFM) is a recombinant, human, full length, coagulation factor VIII that has been produced without the addition of human- or animal-derived plasma proteins, thereby virtually eliminating the risk of transmission of blood-borne pathogens. Octocog alfa-PFM is structurally and functionally very similar to a previously marketed, albumin-containing formulation of the same recombinant factor VIII. The haemostatic efficacy of octocog alfa-PFM was rated excellent or good in the acute treatment of most breakthrough bleeding episodes in adolescents or adults with moderately severe or severe haemophilia A who were receiving prophylaxis with octocog alfa-PFM and who had been previously treated with factor VIII. Most bleeding episodes resolved after one or two infusions of octocog alfa-PFM. Efficacy was similar regardless of the cause or site of the bleeding episode. Similar excellent or good haemostatic efficacy was observed with octocog alfa-PFM in previously treated children aged <6 years with haemophilia A and during perioperative use in patients with haemophilia A undergoing surgical or invasive dental procedures. Octocog alfa-PFM was well tolerated during clinical development and in the 15-month post-marketing period. There were very few adverse events and serious events were rare. The risk for developing inhibitors (antibodies) to factor VIII was very low.

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Year:  2005        PMID: 16392876     DOI: 10.2165/00003495-200565180-00005

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


  9 in total

Review 1.  The hemophilias--from royal genes to gene therapy.

Authors:  P M Mannucci; E G Tuddenham
Journal:  N Engl J Med       Date:  2001-06-07       Impact factor: 91.245

2.  Guidelines on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders.

Authors: 
Journal:  Haemophilia       Date:  2003-01       Impact factor: 4.287

3.  Inhibitor development in patients receiving recombinant factor VIII (Recombinate rAHF/Bioclate): a prospective pharmacovigilance study.

Authors:  B M Ewenstein; E D Gomperts; S Pearson; M E O'Banion
Journal:  Haemophilia       Date:  2004-09       Impact factor: 4.287

4.  Stability of lyophilized and reconstituted plasma/albumin-free recombinant human factor VIII (ADVATE rAHF-PFM).

Authors:  R Parti; A Schoppmann; H Lee; L Yang
Journal:  Haemophilia       Date:  2005-09       Impact factor: 4.287

Review 5.  Pharmacokinetics of coagulation factors: clinical relevance for patients with haemophilia.

Authors:  S Björkman; E Berntorp
Journal:  Clin Pharmacokinet       Date:  2001       Impact factor: 6.447

6.  Economic and epidemiological modelling of full-length antihaemophilic factor (recombinant), plasma/albumin-free method, in previously treated patients with haemophilia A : comparison with B-domain deleted rFVIII, and value of potential viral transmission reduction due to plasma/albumin-free status.

Authors:  David A Sclar; Marc A Evans; Tracy L Skaer; Linda M Robison; Karen C Chung; Nick S Poulios
Journal:  Drugs R D       Date:  2005

Review 7.  State of care for hemophilia in pediatric patients.

Authors:  Elena Santagostino; Alessandro Gringeri; Pier M Mannucci
Journal:  Paediatr Drugs       Date:  2002       Impact factor: 3.022

8.  Hemophilia therapy innovation: development of an advanced category recombinant factor VIII by a plasma/albumin-free method. Proceedings of a Special Symposium at the XIXth Congress of the International Society on Thrombosis and Haemostasis, July 12-18, 2003, Birmingham, UK.

Authors:  B M Ewenstein; P Collins; M D Tarantino; C Negrier; V Blanchette; A D Shapiro; D Baker; G Spotts; M Sensel; S E Yi; E D Gomperts
Journal:  Semin Hematol       Date:  2004-01       Impact factor: 3.851

9.  Clinical evaluation of an advanced category antihaemophilic factor prepared using a plasma/albumin-free method: pharmacokinetics, efficacy, and safety in previously treated patients with haemophilia A.

Authors:  M D Tarantino; P W Collins; C R M Hay; A D Shapiro; R A Gruppo; E Berntorp; G L Bray; S A Tonetta; P C Schroth; A D Retzios; S S Rogy; M G Sensel; B M Ewenstein
Journal:  Haemophilia       Date:  2004-09       Impact factor: 4.287

  9 in total
  1 in total

1.  Allometry of factor VIII and informed scaling of next-generation therapeutic proteins.

Authors:  Matthew P Kosloski; Dipak S Pisal; Donald E Mager; Sathy V Balu-Iyer
Journal:  J Pharm Sci       Date:  2013-04-25       Impact factor: 3.534

  1 in total

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