CC BY 4.0 · TH Open 2024; 08(01): e155-e163
DOI: 10.1055/s-0044-1781466
Original Article

Safety and Efficacy of Recombinant Fusion Protein Linking Coagulation Factor IX with Albumin (rIX-FP) in Previously Untreated Patients with Hemophilia B

Richard Lemons
1   Department of Pediatrics and Primary Children's Hospital, University of Utah, Salt Lake City, Utah, United States
,
Michael Wang
2   Hemophilia and Thrombosis Center, University of Colorado School of Medicine, Colorado, United States
,
Julie Curtin
3   The Children's Hospital at Westmead, New South Wales, Australia
,
Lynda Mae Lepatan
4   Department of Health Research and Pediatrics, Cebu Normal University—Vicente Sotto Memorial Medical Center College of Medicine, Cebu, Philippines
,
Christoph Male
5   Department of Paediatrics, Medical University of Vienna, Vienna, Austria
,
Flora Peyvandi
6   Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Milan, Italy
7   Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy
,
Mario von Depka Prondzinski
8   Werlhof Institute, Hannover, Germany
,
Rongrong Wang
9   CSL Behring, King of Prussia, Pennsylvania, United States
,
William McKeand
9   CSL Behring, King of Prussia, Pennsylvania, United States
,
Wilfried Seifert
10   CSL Behring, Marburg, Germany
,
Johannes Oldenburg
11   Institute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, Medical Faculty, University of Bonn, Bonn, Germany
› Institutsangaben

Abstract

Introduction Recombinant fusion protein linking coagulation factor IX (FIX) with albumin (rIX-FP) has been shown to be an effective, well-tolerated treatment for patients with severe hemophilia B who had previously received factor replacement therapy. This study investigated the safety and efficacy of rIX-FP in previously untreated patients (PUPs).

Methods Patients with moderately severe/severe hemophilia B (≤2% FIX) previously untreated with FIX replacement products received rIX-FP (25–75 IU/kg) prophylaxis weekly or on-demand treatment over ≥50 exposure days (EDs). Primary outcomes were the number of patients who developed FIX inhibitors and mean incremental recovery (IR) following a 50 IU/kg dose of rIX-FP. Secondary outcomes included incidence of adverse events (AEs) and annualized bleeding rates (ABRs).

Results In total, 12 PUPs with a median age of 0 years (range, 0–11 years) were treated with rIX-FP for a median of 50 EDs (6/12 prophylaxis; 6/12 on-demand then prophylaxis). Overall, 11/12 patients did not develop FIX inhibitors; one 11-year-old patient developed an inhibitor against FIX after 8 EDs and was ultimately withdrawn. Mean (standard deviation) IR was 1.2 (0.4, n = 8) (IU/dL)/(IU/kg). Of the 137 treatment-emergent AEs recorded, five were attributed to rIX-FP. On the prophylaxis regimen, median ABR was 1.0 (range, 0–3.9, n = 12). No thromboembolic events or deaths occurred during the study.

Conclusion This study provides data to support the safety and efficacy of rIX-FP in PUPs requiring on-demand or prophylactic treatment for moderately severe/severe hemophilia B, consistent with results in previously treated patients. Overall, 1/12 patients developed an inhibitor against FIX.

Supplementary Material



Publikationsverlauf

Eingereicht: 14. August 2023

Angenommen: 31. Januar 2024

Artikel online veröffentlicht:
26. März 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Srivastava A, Santagostino E, Dougall A. et al; WFH Guidelines for the Management of Hemophilia panelists and co-authors. WFH guidelines for the management of hemophilia, 3rd edition. Haemophilia 2020; 26 (Suppl. 06) 1-158
  • 2 Shapiro A, Potts J, Li S. et al. Association of bleeding tendency with time under target FIX activity levels in severe hemophilia B patients treated with recombinant factor IX Fc fusion protein. Blood 2013; 122: 2349
  • 3 Castaman G. The benefits of prophylaxis in patients with hemophilia B. Expert Rev Hematol 2018; 11 (08) 673-683
  • 4 Fischer K, Lassila R, Peyvandi F. et al; EUHASS participants. Inhibitor development in haemophilia according to concentrate. Four-year results from the European HAemophilia Safety Surveillance (EUHASS) project. Thromb Haemost 2015; 113 (05) 968-975
  • 5 Chitlur M, Warrier I, Rajpurkar M, Lusher JM. Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (1997-2006). Haemophilia 2009; 15 (05) 1027-1031
  • 6 European Medicines Agency. Summary of Product Characteristics. IDELVION. 2023. . Available at: https://www.ema.europa.eu/en/medicines/human/EPAR/idelvion
  • 7 Kenet G, Chambost H, Male C. et al; PROLONG-9FP Investigator Study Group. Long-acting recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP) in children. Results of a phase 3 trial. Thromb Haemost 2016; 116 (04) 659-668
  • 8 Kenet G, Chambost H, Male C. et al. Long-term safety and efficacy of recombinant coagulation factor IX albumin fusion protein (rIX-FP) in previously treated pediatric patients with hemophilia B: Results from a phase 3b extension study. Thromb Haemost 2020; 120 (04) 599-606
  • 9 Mancuso ME, Lubetsky A, Pan-Petesch B. et al. Long-term safety and efficacy of rIX-FP prophylaxis with extended dosing intervals up to 21 days in adults/adolescents with hemophilia B. J Thromb Haemost 2020; 18 (05) 1065-1074
  • 10 Santagostino E, Negrier C, Klamroth R. et al. Safety and pharmacokinetics of a novel recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP) in hemophilia B patients. Blood 2012; 120 (12) 2405-2411
  • 11 Metzner HJ, Weimer T, Kronthaler U, Lang W, Schulte S. Genetic fusion to albumin improves the pharmacokinetic properties of factor IX. Thromb Haemost 2009; 102 (04) 634-644
  • 12 European Medicines Agency. Guidelines on clinical investigation of recombinant and human plasma-derived factor IX products. 2011 . Available at: https://www.ema.europa.eu/en/clinical-investigation-recombinant-and-human-plasma-derived-factor-ix-products-scientific-guideline
  • 13 Male C, Andersson NG, Rafowicz A. et al. Inhibitor incidence in an unselected cohort of previously untreated patients with severe haemophilia B: A PedNet study. Haematologica 2021; 106 (01) 123-129
  • 14 Lillicrap D. Evaluating the potential benefits of the extravascular pool of factor IX. Blood Coagul Fibrinolysis 2021; 32 (01) 68-69
  • 15 Santagostino E, Martinowitz U, Lissitchkov T. et al; PROLONG-9FP Investigators Study Group. Long-acting recombinant coagulation factor IX albumin fusion protein (rIX-FP) in hemophilia B: Results of a phase 3 trial. Blood 2016; 127 (14) 1761-1769
  • 16 Nolan B, Klukowska A, Shapiro A. et al. Final results of the PUPs B-LONG study: Evaluating safety and efficacy of rFIXFc in previously untreated patients with hemophilia B. Blood Adv 2021; 5 (13) 2732-2739
  • 17 Chan AK, Alamelu J, Barnes C. et al. Nonacog beta pegol (N9-GP) in hemophilia B: First report on safety and efficacy in previously untreated and minimally treated patients. Res Pract Thromb Haemost 2020; 4 (07) 1101-1113