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Nonacog beta pegol prophylaxis in children with hemophilia B: safety, efficacy, and neurodevelopmental outcomes for up to 8 years
Author(s): ,
Kevin Shapiro
Affiliations:
Cortica Healthcare and Children’s Hospital Los Angeles, Westlake Village, California, USA
,
Helle Holst
Affiliations:
Novo Nordisk A/S, Copenhagen, Denmark
,
Pernille Højlund Nielsen
Affiliations:
Novo Nordisk A/S, Copenhagen, Denmark
,
Anthony K.C. Chan
Affiliations:
Department of Paediatrics, McMaster Centre for Transfusion Research, McMaster Children’s Hospital, McMaster University, Hamilton, Ontario, Canada
,
Manuel Carcao
Affiliations:
Division of Haematology/Oncology, Department of Paediatrics, the Hospital for Sick Children, Toronto, Ontario, Canada
,
Christine Mrakotsky
Affiliations:
Departments of Neurology & Psychiatry, Boston Children’s Hospital, Harvard Medical School, Boston, Massachusetts, USA
Karin S. Walsh
Affiliations:
Center for Neuroscience and Behavioral Medicine, Children’s National Hospital and the George Washington University School of Medicine and Health Sciences, Washington, DC, USA
Karin S. Walsh, Children’s National Hospital, 14245 Shady Grove Road, Suite 350, Rockville, MD 20850, USA.
ISTH Academy. Presenters F. 02/01/24; 417426
Faculty / Presenters
Faculty /  Presenters
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Background

Nonacog beta pegol (N9-GP) is an extended half-life PEGylated factor (F)IX product with established efficacy and short-term safety in persons with hemophilia B (HB). Long-term safety has been evaluated for polyethylene glycol exposure but not N9-GP.

Objectives

To assess safety, neurodevelopmental, and efficacy outcomes of children with HB receiving N9-GP prophylaxis across 2 open-label, single-arm, phase 3 studies: paradigm5 (previously treated patients [PTPs]) and paradigm6 (previously untreated patients [PUPs]) in this interim analysis.

Methods

PTPs (aged ≤12 years) and PUPs (aged <6 years) with severe/moderate (≤2% FIX level) HB were recruited to N9-GP prophylaxis (40 IU/kg once weekly) in paradigm5 and paradigm6, respectively. Safety assessments included FIX inhibitor incidence, adverse events, neurocognitive and neurologic outcomes, polyethylene glycol concentration in plasma, and medical events of special interest. Efficacy endpoints included bleeds, N9-GP hemostatic effect, and FIX consumption.

Results

Overall, 25 patients in paradigm5 and 50 patients in paradigm6 received N9-GP and were followed for up to 8 and 6 years, respectively. No inhibitory antibodies were reported in PTPs; 4 of the 50 PUPs developed inhibitors. Extensive evaluation revealed no neurocognitive or neurologic concerns with N9-GP use in children during the study period. Across both studies, few adverse events were reported as possibly related to N9-GP. High hemostatic response rate, high treatment adherence, low annualized bleeding rates, and no new target joints were reported.

Conclusion

These data provide the longest follow-up for an extended half-life FIX and confirm the long-term efficacy of N9-GP prophylaxis in children with HB with no observed neurocognitive or neurologic safety concerns.

Abstract

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Abstract

Long-term safety data for clotting factor concentrates joined to polyethylene glycol molecules are limited. Paradigm 5/6 assesses the long-term safety and efficacy of nonacog beta pegol in children with hemophilia B. Safety data showed no impact of long-term nonacog beta pegol on neurologic or neurocognitive development. Efficacy results were robust, with high treatment adherence and low bleeding rates.

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