Literature DB >> 31039049

Current and emerging biologics for the treatment of hemophilia.

Giancarlo Castaman1, Silvia Linari1.   

Abstract

INTRODUCTION: The development of new biologic agents able to restore thrombin generation has become the focus of innovation in hemophilia management. There is growing interest in the proposal of novel, non-replacement therapy with alternative mechanisms of action and route of administration, hoping to solve still unmet needs in treatment of hemophilic patients with or without inhibitors. AREAS COVERED: The review describes the new molecules, in particular the bi-specific antibody mimicking the coagulation function of FVIII and/or those which work by inhibiting the natural anticoagulants, their mechanism of action and the results of ongoing clinical trials. EXPERT OPINION: Exciting results in enhancing the protection against bleeding and improving quality of life are emerging from clinical trials. However, these molecules with their mechanisms of action also open new problems. Treatment of bleeding and management of surgery in subjects with a rebalanced hemostasis may be difficult, especially for the lack of laboratory tests perfectly reflecting the in vivo coagulation status. A careful surveillance is required to evaluate the risk of thrombotic complication in patients with rebalanced hemostasis, in addition to understand whether these new products offer the same protection on joints as regular prophylaxis with the missing clotting factors.

Entities:  

Keywords:  Anti-TFPI; antithrombin suppression; bi-specific antibody; bleeding; hemophilia; inhibitors; prophylaxis; rebalanced hemostasis

Year:  2019        PMID: 31039049     DOI: 10.1080/14712598.2019.1614163

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  4 in total

1.  Current Choices and Management of Treatment in Persons with Severe Hemophilia A without Inhibitors: A Mini-Delphi Consensus.

Authors:  Antonio Coppola; Massimo Franchini; Giovanni Pappagallo; Alessandra Borchiellini; Raimondo De Cristofaro; Angelo Claudio Molinari; Rita Carlotta Santoro; Cristina Santoro; Annarita Tagliaferri
Journal:  J Clin Med       Date:  2022-02-02       Impact factor: 4.241

2.  Nonneutralizing FVIII-specific antibody signatures in patients with hemophilia A and in healthy donors.

Authors:  Helmut Schweiger; Judit Rejtő; Christoph J Hofbauer; Verena Berg; Peter Allacher; Karl Zwiauer; Clemens Feistritzer; Gerhard Schuster; Cihan Ay; Birgit M Reipert; Ingrid Pabinger
Journal:  Blood Adv       Date:  2022-02-08

Review 3.  Concomitant Use of rFVIIa and Emicizumab in People with Hemophilia A with Inhibitors: Current Perspectives and Emerging Clinical Evidence.

Authors:  Silvia Linari; Giancarlo Castaman
Journal:  Ther Clin Risk Manag       Date:  2020-05-22       Impact factor: 2.423

4.  The factor VIII treatment history of non-severe hemophilia A.

Authors:  Amal Abdi; Fabienne R Kloosterman; Corien L Eckhardt; Christoph Male; Giancarlo Castaman; Kathelijn Fischer; Erik A M Beckers; Marieke J H A Kruip; Kathelijne Peerlinck; Maria Elisa Mancuso; Cristina Santoro; Charles R Hay; Helen Platokouki; Johanna G van der Bom; Samantha C Gouw; Karin Fijnvandraat; Dan P Hart
Journal:  J Thromb Haemost       Date:  2020-09-28       Impact factor: 16.036

  4 in total

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