BAY 94-9027 prophylaxis is efficacious and well tolerated for up to >5 years with extended dosing intervals: PROTECT VIII extension interim results

Shadan Lalezari, Mark T. Reding, Ingrid Pabinger, Pal Andre Holme, Claude Negrier, Pavani Chalasani, Ho Jin Shin, Maria Wang, Despina Tseneklidou-Stoeter, Monika Maas Enriquez

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Introduction: BAY 94-9027 is an extended‒half-life, site-specifically PEGylated, B-domain‒deleted recombinant factor VIII (FVIII). The PROTECT VIII main study demonstrated efficacy of bleed control using extended-interval prophylaxis with BAY 94-9027 for 36 weeks. Aim: To report long-term efficacy and safety of prophylaxis with BAY 94-9027 in a descriptive analysis of the ongoing PROTECT VIII extension with a total treatment time of up to >5 years. Methods: Previously treated males aged 12-65 years with severe haemophilia A who completed the PROTECT VIII main study were eligible for the open-label extension. Patients received on-demand treatment or prophylaxis (30‒40 IU/kg twice weekly, 45‒60 IU/kg every 5 days, or 60 IU/kg every 7 days) and could switch regimens as needed. Results: Patients (N = 121; on demand, n = 14; prophylaxis, n = 107) accumulated a median (range) of 3.9 years (297‒1965 days) and 223 (23‒563) total exposure days by 31 January 2018. During the extension, median (quartile [Q]1; Q3) annualized bleeding rates (ABRs) for total bleeds were 1.6 (0.3; 4.6) for patients receiving prophylaxis and 34.1 (20.3; 36.6) for patients receiving on-demand treatment. ABRs for twice-weekly (n = 23), every-5-days (n = 33), every-7-days (n = 23) and variable frequency (n = 28) treatments were 1.7, 1.2, 0.7 and 3.1, respectively. Of prophylaxis patients, 20.6% were bleed-free throughout the extension (median time, 3.2 years), and 44.5% were bleed-free during the last 6 months. No patients developed FVIII inhibitors. Conclusions: BAY 94-9027 prophylaxis was efficacious and well tolerated with dosing intervals up to every 7 days for a median (range) of 3.9 years (0.8-5.4 years).

Original languageEnglish (US)
Pages (from-to)1011-1019
Number of pages9
JournalHaemophilia
Volume25
Issue number6
DOIs
StatePublished - Nov 1 2019

Bibliographical note

Funding Information:
I. Pabinger: has received honoraria for lectures and advisory board meetings from Bayer, CSL Behring, Pfizer, Novo Nordisk, Sobi and Shire, and has received unrestricted research grants from CSL Behring and Novo Nordisk.

Funding Information:
M. T. Reding: has received honoraria for participation on advisory boards and/or speakers bureaus from Bayer, Bioverativ, Genentech, Novo Nordisk, Pfizer and Shire, and grant funding from Bayer and Biomarin.

Publisher Copyright:
© 2019 The Authors. Haemophilia published by John Wiley & Sons Ltd

Keywords

  • clinical trial
  • factor VIII
  • haemophilia A
  • intravenous infusions
  • recombinant proteins

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