Literature DB >> 27891721

Extended half-life pegylated, full-length recombinant factor VIII for prophylaxis in children with severe haemophilia A.

E S Mullins1, O Stasyshyn2, M T Alvarez-Román3, D Osman4, R Liesner5, W Engl6, M Sharkhawy6, B E Abbuehl6.   

Abstract

INTRODUCTION: Primary factor VIII (FVIII) prophylaxis is the optimal treatment in children with severe haemophilia A. They are expected to benefit from extended half-life (T1/2 ) FVIII coverage by reduced infusion frequency while maintaining haemostatic efficacy. AIMS: To determine immunogenicity, pharmacokinetics (PK), efficacy, safety and quality of life of prophylaxis with a polyethylene glycol (peg)-ylated FVIII (BAX 855) based on full-length recombinant FVIII (ADVATE) in paediatric previously treated patients (PTPs) with severe haemophilia A.
METHODS: PTPs <12 years without history of FVIII inhibitors received twice-weekly infusions of 50 ± 10 IU kg-1 BAX 855 for ≥50 exposure days. Prophylactic dose increases to ≤80 IU kg-1 were allowed under predefined conditions. PK was evaluated after single infusions of 60 ± 5 IU kg-1 .
RESULTS: T1/2 and mean residence time were extended 1.3- to 1.5-fold compared to ADVATE (n = 31), depending on the analysis used. The point estimate for the mean annualized bleeding rate in 66 subjects receiving a median of 1.9 weekly infusions of 51.3 IU kg-1 of BAX 855 each was 3.04 (median 2.0); 1.10 (median 0) for joint and 1.16 (median 0) for spontaneous bleeds. Overall, 38% of subjects had zero bleeds. No bleeds were severe. Haemostatic efficacy was rated excellent or good for 90% of bleeds; 91% were treated with one or two infusions. In 8/14 subjects all target joints resolved. No subject developed FVIII inhibitors or persistent binding antibodies that affected safety or efficacy. No adverse reactions occurred.
CONCLUSION: Twice-weekly prophylaxis with BAX 855 was safe and efficacious in paediatric PTPs with severe haemophilia A.
© 2016 Baxalta Innovations GmbH. Haemophilia Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  children; extended half-life FVIII; prophylaxis

Mesh:

Substances:

Year:  2016        PMID: 27891721     DOI: 10.1111/hae.13119

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


  22 in total

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Authors:  Thierry Lambert; Gary Benson; Gerry Dolan; Cedric Hermans; Victor Jiménez-Yuste; Rolf Ljung; Massimo Morfini; Silva Zupančić-Šalek; Elena Santagostino
Journal:  Ther Adv Hematol       Date:  2018-09-06

Review 2.  Factor VIII replacement is still the standard of care in haemophilia A.

Authors:  Louis Aledort; Pier Mannuccio Mannucci; Wolfgang Schramm; Michael Tarantino
Journal:  Blood Transfus       Date:  2019-12-11       Impact factor: 3.443

Review 3.  Extended Half-Life Factor VIII and Factor IX Preparations.

Authors:  Lukas Graf
Journal:  Transfus Med Hemother       Date:  2018-03-21       Impact factor: 3.747

Review 4.  Clotting factor concentrates for preventing bleeding and bleeding-related complications in previously treated individuals with haemophilia A or B.

Authors:  Omotola O Olasupo; Megan S Lowe; Ashma Krishan; Peter Collins; Alfonso Iorio; Davide Matino
Journal:  Cochrane Database Syst Rev       Date:  2021-08-18

5.  Rurioctocog alfa pegol PK-guided prophylaxis in hemophilia A: results from the phase 3 PROPEL study.

Authors:  Robert Klamroth; Jerzy Windyga; Vlad Radulescu; Peter W Collins; Oleksandra Stasyshyn; Hishamshah Mohd Ibrahim; Werner Engl; Srilatha D Tangada; William Savage; Bruce Ewenstein
Journal:  Blood       Date:  2021-04-01       Impact factor: 22.113

Review 6.  Novel therapies and current clinical progress in hemophilia A.

Authors:  Pauline Balkaransingh; Guy Young
Journal:  Ther Adv Hematol       Date:  2017-12-28

7.  Mechanistic Insights into Factor VIII Immune Tolerance Induction via Prenatal Cell Therapy in Hemophilia A.

Authors:  Martin Rodriguez; Christopher D Porada; Graҫa Almeida-Porada
Journal:  Curr Stem Cell Rep       Date:  2019-11-20

8.  PROTECT VIII kids extension study: Long-term safety and efficacy of BAY 94-9027 (damoctocog alfa pegol) in children with severe haemophilia A.

Authors:  Maria Elisa Mancuso; Tina Biss; Kathelijn Fischer; Monika Maas Enriquez; MacGregor Steele; Maria Wang; Despina Tseneklidou-Stoeter; Sanjay Ahuja; Gili Kenet
Journal:  Haemophilia       Date:  2021-03-16       Impact factor: 4.287

Review 9.  Outcome of Clinical Trials with New Extended Half-Life FVIII/IX Concentrates.

Authors:  Maria Elisa Mancuso; Elena Santagostino
Journal:  J Clin Med       Date:  2017-03-28       Impact factor: 4.241

10.  Turoctocog alfa pegol provides effective management for major and minor surgical procedures in patients across all age groups with severe haemophilia A: Full data set from the pathfinder 3 and 5 phase III trials.

Authors:  Alberto Tosetto; Anne Neff; Steven R Lentz; Elena Santagostino; Laszlo Nemes; Jameela Sathar; Karina Meijer; Pratima Chowdary; Chunduo Shen; Andrea Landorph; Kingsley Hampton
Journal:  Haemophilia       Date:  2020-04-15       Impact factor: 4.287

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