Literature DB >> 25315324

Pharmacokinetic and pharmacodynamic properties of plasma-derived vs. recombinant factor IX in patients with hemophilia B: a prospective crossover study.

J Alamelu1, D Bevan, B Sorensen, S Rangarajan.   

Abstract

BACKGROUND: Effective treatment of acute bleeding episodes in patients with hemophilia B relies on factor IX recovery, with higher levels being more desirable, whereas prevention of bleeds with a prophylactic regimen depends on the half-life of the product. Lower recovery values have been reported following administration of recombinant FIX (rFIX) than following administration of plasma-derived FIX (pdFIX).
OBJECTIVES: To compare the pharmacokinetic and pharmacodynamic properties of rFIX and pdFIX in patients with hemophilia B.
METHODS: A prospective crossover study of nine patients with moderate to severe hemophilia B was performed. Following a washout period, 50 U kg(-1) FIX was administered, and blood samples were taken as per protocol up to 48 h postinfusion. Paired data were analyzed with the Wilcoxon signed rank test.
RESULTS: Mean peak recovery at 10 min postinfusion was 62.14 IU dL(-1) with pdFIX and 52.7 IU dL(-1) with rFIX (P = 0.08). Mean half-life was 16.6 h with pdFIX and 17.5 h with rFIX (P = 0.55). Maximum peak thrombin generation (PTG) was 35.9 nm with pdFIX and 28.9 nm with rFIX (P = 0.21). Administration of rFIX resulted in early PTG, whereas administration of pdFIX resulted in slightly later and sustained PTG. At 48 h, PTG was similar with pdFIX (19.0 nm) and rFIX (19.4 nm) (P = 0.91).
CONCLUSIONS: Patients experienced better recovery with pdFIX than with rFIX. pdFIX and rFIX had similar half-lives. Maximum PTG was higher for pdFIX; however, this difference did not reach statistical significance. The clinical impact of the slightly increased, delayed and sustained PTG with pdFIX requires further investigation.
© 2014 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  factor IX; half-life; hemophilia B; pharmacodynamics; pharmacokinetics

Mesh:

Substances:

Year:  2014        PMID: 25315324     DOI: 10.1111/jth.12756

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  5 in total

1.  Orphan Drug Use in Patients With Rare Diseases: A Population-Based Cohort Study.

Authors:  Francesca Gorini; Michele Santoro; Anna Pierini; Lorena Mezzasalma; Silvia Baldacci; Elena Bargagli; Alessandra Boncristiano; Maurizia Rossana Brunetto; Paolo Cameli; Francesco Cappelli; Giancarlo Castaman; Barbara Coco; Maria Alice Donati; Renzo Guerrini; Silvia Linari; Vittoria Murro; Iacopo Olivotto; Paola Parronchi; Francesca Pochiero; Oliviero Rossi; Barbara Scappini; Andrea Sodi; Alessandro Maria Vannucchi; Alessio Coi
Journal:  Front Pharmacol       Date:  2022-05-16       Impact factor: 5.988

2.  Issues in assessing products for the treatment of hemophilia - the intersection between efficacy, economics, and ethics.

Authors:  Albert Farrugia; Declan Noone; Uwe Schlenkrich; Steffen Schlenkrich; Brian O'Mahony; Josephine Cassar
Journal:  J Blood Med       Date:  2015-06-15

Review 3.  Using pharmacokinetics for tailoring prophylaxis in people with hemophilia switching between clotting factor products: A scoping review.

Authors:  Jacky K Yu; Alfonso Iorio; Andrea N Edginton
Journal:  Res Pract Thromb Haemost       Date:  2019-05-20

Review 4.  New developments in the management of moderate-to-severe hemophilia B.

Authors:  Moniba Nazeef; John P Sheehan
Journal:  J Blood Med       Date:  2016-04-01

Review 5.  Once-weekly prophylactic dosing of recombinant factor IX improves adherence in hemophilia B.

Authors:  Claudia Djambas Khayat
Journal:  J Blood Med       Date:  2016-11-30
  5 in total

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