Literature DB >> 29582525

Clinical experience with moroctocog alfa (AF-CC) in younger paediatric patients with severe haemophilia A: Two open-label studies.

L Rusen1, K Kavakli2, J Korth-Bradley3, F Huard4, P Rendo3, J Fuiman3, J A Baumann3, L Smith3, C Alvey5, J Rupon3.   

Abstract

INTRODUCTION: The pharmacokinetics (PK), efficacy and safety of moroctocog alfa (AF-CC) have been demonstrated in haemophilia A patients aged ≥6 years. AIM: These studies aimed to further describe moroctocog alfa (AF-CC) experience in paediatric patients (<12 years) with severe haemophilia A (FVIII:C < 1%).
METHODS: Two prospective, open-label studies enrolled patients aged <12 years: one study with 37 previously treated patients (PTPs) and another with 23 previously untreated patients (PUPs). All patients initially received 50 IU/kg of moroctocog alfa (AF-CC) to evaluate either recovery alone, or with other PK parameters (6 to <12 years) before continuing treatment for 100 exposure days (EDs) or 24 months.
RESULTS: At baseline, mean (±SD) recovery ranged between 1.32 ± 0.65 (PUPs aged <2 years) and 2.13 ± 0.82 (PTPs aged 6 to <12 years). The mean (±SD) half-life was 9.12 ± 1.94 hours in PTPs aged 6 to <12 years. No new safety signals were detected in either study, 2 transient lower titre inhibitors occurred in PTPs while 8 inhibitors (3 low and 5 high titre) were detected in PUPs. Most bleeding episodes resolved with one infusion (94% [893/954]). The annualised bleeding rate (ABR) in the PTP study was 27.5 and 4.2 for patients reporting an on-demand and routine prophylaxis regimen at baseline, respectively. In the PUP study, the overall ABR was 5.9.
CONCLUSION: Moroctocog alfa (AF-CC) had expected PK findings (lower recovery in young children compared with older children) along with being safe and efficacious in a population of young severe haemophilia A patients.
© 2018 The Authors. Haemophilia Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  clinical trial; factor replacement; pharmacokinetics; previously treated patients; previously untreated patients; recombinant factor VIII

Mesh:

Substances:

Year:  2018        PMID: 29582525     DOI: 10.1111/hae.13466

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


  1 in total

1.  Safety and efficacy of turoctocog alfa in the prevention and treatment of bleeds in previously untreated paediatric patients with severe haemophilia A: Results from the guardian 4 multinational clinical trial.

Authors:  Hassan Yaish; Tadashi Matsushita; Meriem Belhani; Víctor Jiménez-Yuste; Kaan Kavakli; Lars Korsholm; Irina Matytsina; Claire Philipp; Kirsten Reichwald; Runhui Wu
Journal:  Haemophilia       Date:  2019-12-09       Impact factor: 4.287

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.