Literature DB >> 24762271

Novel products for haemostasis - current status.

J Oldenburg1, T Albert.   

Abstract

Currently, new clotting factor concentrates are becoming available or are in advanced clinical studies that will significantly improve the treatment of patients with Haemophilia A or Haemophilia B. Various technologies are applied to extend half-life and/or allow for alternative routes of administration, e.g. subcutaneous route. Today, the advances for recombinant factor IX are significantly with half-life extensions to up to 100 h, allowing substitution intervals of 1-2 weeks. For recombinant factor VIII (FVIII) products the effect so far is only moderate, as the half-life extension is limited to about 15-18 h by the clearance of FVIII through its binding to von Willebrand factor. However, novel products applying new technologies with significantly extended half-life are already at the horizont, as a bispecific antibody that mimics FVIII. The pharmacokinetic improvements of the new products will lead to a revision of our current treatment regimens, with regard to intended trough levels, number of tolerated bleeds and likely will drive a greater individualization of regimens. Clearly, the potential of anti drug antibody response for these modified proteins must not be higher than with our current products. Another challenge are the increasingly diverse biochemical characteristics of the new products, that have to be considered when determining potencies and also when monitoring treatment in patients with the various available assays. Despite these challenges, the new products will significantly improve treatment and quality of life for our patients with haemophilia.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  haemophilia; half-life; long-acting clotting factor; novel products; pharmacokinetic

Mesh:

Substances:

Year:  2014        PMID: 24762271     DOI: 10.1111/hae.12428

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


  9 in total

1.  Generation of hyperfunctional recombinant human factor IX variants expressed in human cell line SK-Hep-1.

Authors:  Aline Sousa Bomfim; Marcela Cristina Corrêa de Freitas; Virgínia Picanço Castro; Mario Abreu Soares Neto; Ricardo Pádua; Dimas Tadeu Covas; Elisa Maria Sousa Russo
Journal:  Biotechnol Lett       Date:  2020-11-01       Impact factor: 2.461

2.  Peptides identified on monocyte-derived dendritic cells: a marker for clinical immunogenicity to FVIII products.

Authors:  Wojciech Jankowski; Yara Park; Joseph McGill; Eugene Maraskovsky; Marco Hofmann; Vincent P Diego; Bernadette W Luu; Tom E Howard; Roberta Kellerman; Nigel S Key; Zuben E Sauna
Journal:  Blood Adv       Date:  2019-05-14

Review 3.  [Factor XIII : Pharmacodynamic and pharmacokinetic characteristics].

Authors:  E H Adam; S Kreuer; K Zacharowski; C F Weber; R Wildenauer
Journal:  Anaesthesist       Date:  2017-01       Impact factor: 1.041

Review 4.  Towards personalised therapy for von Willebrand disease: a future role for recombinant products.

Authors:  Emmanuel J Favaloro
Journal:  Blood Transfus       Date:  2016-03-22       Impact factor: 3.443

Review 5.  Novel approaches to hemophilia therapy: successes and challenges.

Authors:  Valder R Arruda; Bhavya S Doshi; Benjamin J Samelson-Jones
Journal:  Blood       Date:  2017-10-10       Impact factor: 22.113

Review 6.  Aspects of prophylactic treatment of hemophilia.

Authors:  Rolf Ljung
Journal:  Thromb J       Date:  2016-10-04

Review 7.  Clinical utility and impact of the use of the chromogenic vs one-stage factor activity assays in haemophilia A and B.

Authors:  Richard A Marlar; Karin Strandberg; Midori Shima; Dorothy M Adcock
Journal:  Eur J Haematol       Date:  2019-11-13       Impact factor: 2.997

Review 8.  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

9.  Long-term safety and efficacy of N8-GP in previously treated adults and adolescents with hemophilia A: Final results from pathfinder2.

Authors:  Paul Giangrande; Faraizah Abdul Karim; Laszlo Nemes; Chur Woo You; Andrea Landorph; Milan S Geybels; Nicola Curry
Journal:  J Thromb Haemost       Date:  2020-09       Impact factor: 5.824

  9 in total

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