Literature DB >> 29633467

Defining extended half-life rFVIII-A critical review of the evidence.

J Mahlangu1, G Young2, C Hermans3, V Blanchette4, E Berntorp5, E Santagostino6.   

Abstract

INTRODUCTION: Recent haemophilia treatment advances include new recombinant FVIII (rFVIII) products with improved pharmacokinetic (PK) properties that aim to reduce the burden of prophylaxis. These treatments are commonly referred to as extended half-life rFVIII products (EHL rFVIII). There is no uniform definition of what constitutes an EHL rFVIII. Such a definition would help physicians, patients and funders understand the properties of standard and EHL rFVIIIs and thus provide clarity when selecting an EHL in clinical settings. AIM: To critically assess the published evidence on new and emerging rFVIII products in order to propose a definition to classify EHL rFVIIIs.
METHODS: We systematically searched PubMed, EMBASE and regulatory authorities (FDA/EMA/Health Canada) websites for publications and regulatory submissions describing prospective crossover PK studies evaluating rFVIIIs that demonstrate improved PK parameters in adults and adolescents with severe haemophilia A.
RESULTS: Following critical analyses of the published data, we developed a holistic approach to defining rFVIIIs as EHLs, which requires all of the following: (i) using technology designed to extend rFVIII half-life; (ii) lacking bioequivalence with a standard rFVIII comparator-above the FDA/EMA cut-off of 125% for the 90% confidence intervals for area under the curve ratio; and (iii) having an extended half-life ratio measured in a PK comparator crossover study.
CONCLUSION: In this systematic review, a pragmatic definition of EHL rFVIII has been proposed that should provide better clarity in clinical discussions surrounding the appropriate use of rFVIII products. At present, only products using PEGylation or Fc fusion half-life extension technology meet the proposed criteria for definition of EHL rFVIII.
© 2018 The Authors. Haemophilia Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  bioequivalence; extended half-life; haemophilia A; prophylaxis; recombinant factor VIII

Mesh:

Substances:

Year:  2018        PMID: 29633467     DOI: 10.1111/hae.13438

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  16 in total

Review 1.  Treatment Options in Hemophilia.

Authors:  Wolfgang Miesbach; Joachim Schwäble; Markus M Müller; Erhard Seifried
Journal:  Dtsch Arztebl Int       Date:  2019-11-22       Impact factor: 5.594

Review 2.  How do we optimally utilize factor concentrates in persons with hemophilia?

Authors:  Ming Y Lim
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10

3.  Real-World Clinical Outcomes and Replacement Factor VIII Consumption in Patients with Haemophilia A in Italy: A Comparison between Prophylaxis Pre and Post Octocog Alfa (BAY 81-8973).

Authors:  Paolo Angelo Cortesi; Giovanni Di Minno; Ezio Zanon; Gaetano Giuffrida; Rita Carlotta Santoro; Renato Marino; Lucia Sara D'Angiolella; Ippazio Cosimo Antonazzo; Ginevra Squassabia; Francesco Clemente; Danilo Di Laura; Ernesto Cimino; Samantha Pasca; Daniela Nicolosi; Lorenzo Giovanni Mantovani
Journal:  J Clin Med       Date:  2022-06-15       Impact factor: 4.964

4.  FVIII half-life extension by coadministration of a D'D3 albumin fusion protein in mice, rabbits, rats, and monkeys.

Authors:  Sabine Pestel; Hans-Wilhelm Beltz; Philipp Claar; Holger Lind; Marcel Mischnik; Elmar Raquet; Arna Andrews; Jason Simmonds; Vesna Tomasetig; Steven K Dower; Anna Tjärnlund-Wolf; Stefan Schulte; Peter M Schmidt; Thomas Weimer
Journal:  Blood Adv       Date:  2020-05-12

5.  Impact of novel hemophilia therapies around the world.

Authors:  Margareth C Ozelo; Gabriela G Yamaguti-Hayakawa
Journal:  Res Pract Thromb Haemost       Date:  2022-04-12

6.  Health-related quality-of-life and treatment satisfaction of individuals with hemophilia A treated with turoctocog alfa pegol (N8-GP): a new recombinant extended half-life FVIII.

Authors:  Susan Kearney; Leslie J Raffini; Tan P Pham; Xin Ying Lee; Sylvia von Mackensen; Andrea Landorph; Hideyuki Takedani; Johannes Oldenburg
Journal:  Patient Prefer Adherence       Date:  2019-04-09       Impact factor: 2.711

Review 7.  Recombinant factor VIII Fc for the treatment of haemophilia A.

Authors:  Cedric Hermans; Maria Elisa Mancuso; Beatrice Nolan; K John Pasi
Journal:  Eur J Haematol       Date:  2021-03-31       Impact factor: 2.997

Review 8.  Bispecific Antibodies and Advances in Non-Gene Therapy Options in Hemophilia.

Authors:  Midori Shima
Journal:  Res Pract Thromb Haemost       Date:  2020-04-28

9.  A mutated factor X activatable by thrombin corrects bleedings in vivo in a rabbit model of antibody-induced hemophilia A.

Authors:  Toufik Abache; Alexandre Fontayne; Dominique Grenier; Emilie Jacque; Alain Longue; Anne-Sophie Dezetter; Béatrice Souilliart; Guillaume Chevreux; Damien Bataille; Sami Chtourou; Jean-Luc Plantier
Journal:  Haematologica       Date:  2020-09-01       Impact factor: 9.941

Review 10.  Population Pharmacokinetics of Clotting Factor Concentrates and Desmopressin in Hemophilia.

Authors:  Tim Preijers; Lisette M Schütte; Marieke J H A Kruip; Marjon H Cnossen; Frank W G Leebeek; Reinier M van Hest; Ron A A Mathôt
Journal:  Clin Pharmacokinet       Date:  2021-01       Impact factor: 6.447

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.