PROTECT VIII kids extension study: Long-term safety and efficacy of BAY 94-9027 (damoctocog alfa pegol) in children with severe haemophilia A

被引:9
作者
Mancuso, Maria Elisa [1 ,2 ]
Biss, Tina [3 ]
Fischer, Kathelijn [4 ]
Enriquez, Monika Maas [5 ]
Steele, MacGregor [6 ]
Wang, Maria [7 ]
Tseneklidou-Stoeter, Despina [8 ]
Ahuja, Sanjay [9 ]
Kenet, Gili [10 ,11 ]
机构
[1] Fdn IRCCS Ca Granda, Osped Maggiore Policlin, Milan, Italy
[2] IRCCS Humanitas Res Hosp, Ctr Thrombosis & Hemorrhag Dis, Milan, Italy
[3] Newcastle Upon Tyne Hosp NHS Fdn Trust, Newcastle Upon Tyne, Tyne & Wear, England
[4] Univ Utrecht, Univ Med Ctr Utrecht, Van Creveldklin, Utrecht, Netherlands
[5] Bayer, Wuppertal, Germany
[6] Univ Calgary, Alberta Childrens Hosp, Cumming Sch Med, Calgary, AB, Canada
[7] Bayer, Whippany, NJ USA
[8] Bayer, Berlin, Germany
[9] Case Western Reserve Univ, Rainbow Babies & Childrens Hosp, Univ Hosp, Rainbow Hemostasis & Thrombosis Ctr,Sch Med, Cleveland, OH 44106 USA
[10] Chaim Sheba Med Ctr, Israel Natl Hemophilia Ctr, Tel Hashomer, Israel
[11] Tel Aviv Univ, Amalia Biron Thrombosis Res Inst, Tel Aviv, Israel
关键词
adolescents; children; damoctocog alfa pegol; FVIII; haemophilia A; polyethylene glycol; prophylaxis; RECOMBINANT FACTOR-VIII; EXTENDED HALF-LIFE;
D O I
10.1111/hae.14294
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: BAY 94-9027 (damoctocog alfa pegol; an extended half-life PEGylated recombinant factor VIII [FVIII]) demonstrated efficacy and safety in previously treated paediatric patients (PTPs) aged <12 years with severe haemophilia A in the PROTECT VIII Kids study (NCT01775618). Aim: To evaluate the long-term safety of BAY 94-9027 in PTPs aged <12 years at enrolment. Methods: In the PROTECT VIII Kids study, boys <12 years with severe haemophilia A were enrolled in two age cohorts (6-<12 years and <6 years) and treated prophylactically twice weekly, every 5 days or every 7 days, with BAY 94-9027 for >= 50 exposure days (EDs). Patients who had completed >= 50 EDs and >= 6 months in the main study or 12-week safety expansion study were eligible to participate in the extension. Primary safety variable was frequency of inhibitor development; main efficacy variable was annualised bleeding rate (ABR). Results: Of 73 PTPs from the main/expansion studies, 59 (81%) entered the extension phase for a median (range) duration of 5.0 (0.4-5.9) years. Overall, 39 patients completed >= 5 years of treatment. No patients developed FVIII inhibitors/anti-PEG antibodies, and two patients aged <6 years discontinued. Median ABR for total bleeds was 1.5 (<6 years) and 1.9 (6-<12 years). Total ABR improved in the extension vs. the main study. In the last 12 months of treatment, median spontaneous ABR was 0.0 in both age groups. Conclusions: BAY 94-9027 showed long-term safety and efficacy for the prevention and treatment of bleeds in younger and older paediatric patients with severe haemophilia A.
引用
收藏
页码:434 / 444
页数:11
相关论文
共 16 条
  • [1] Novel therapies and current clinical progress in hemophilia A
    Balkaransingh, Pauline
    Young, Guy
    [J]. THERAPEUTIC ADVANCES IN HEMATOLOGY, 2018, 9 (02) : 49 - 61
  • [2] Advances and challenges for hemophilia gene therapy
    Batty, Paul
    Lillicrap, David
    [J]. HUMAN MOLECULAR GENETICS, 2019, 28 (R1) : R95 - R101
  • [3] PEGylated biologics in haemophilia treatment: Current understanding of their long-term safety
    Baumann, Andreas
    [J]. HAEMOPHILIA, 2020, 26 (01) : E11 - E13
  • [4] Phase I study of BAY 94-9027, a PEGylated B-domain-deleted recombinant factor VIII with an extended half-life, in subjects with hemophilia A
    Coyle, T. E.
    Reding, M. T.
    Lin, J. C.
    Michaels, L. A.
    Shah, A.
    Powell, J.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2014, 12 (04) : 488 - 496
  • [5] Escobar MA., 2019, BLOOD, V134
  • [6] Establishing the Prevalence and Prevalence at Birth of Hemophilia in Males A Meta-analytic Approach Using National Registries
    Iorio, Alfonso
    Stonebraker, Jeffrey S.
    Chambost, Herve
    Makris, Michael
    Coffin, Donna
    Herr, Christine
    Germini, Federico
    Stonebraker, Jeffrey S.
    Iorio, Alfonso
    Byams, Vanessa
    El-Ekiaby, Magdy
    Makris, Michael
    O'Hara, Jamie
    Pierce, Glenn F.
    Weill, Alain
    [J]. ANNALS OF INTERNAL MEDICINE, 2019, 171 (08) : 540 - +
  • [7] Outcome of Clinical Trials with New Extended Half-Life FVIII/IX Concentrates
    Mancuso, Maria Elisa
    Santagostino, Elena
    [J]. JOURNAL OF CLINICAL MEDICINE, 2017, 6 (04)
  • [8] Rational design of a fully active, long-acting PEGylated factor VIII for hemophilia A treatment
    Mei, Baisong
    Pan, Clark
    Jiang, Haiyan
    Tjandra, Hendri
    Strauss, Jonathan
    Chen, Yaoqi
    Liu, Tongyao
    Zhang, Xin
    Severs, Joanne
    Newgren, Jim
    Chen, Jianmin
    Gu, Jian-Ming
    Subramanyam, Babu
    Fournel, Michael A.
    Pierce, Glenn F.
    Murphy, John E.
    [J]. BLOOD, 2010, 116 (02) : 270 - 279
  • [9] Safety and efficacy of a glycoPEGylated rFVIII (turoctocog alpha pegol, N8-GP) in paediatric patients with severe haemophilia A
    Meunier, Sandrine
    Alamelu, Jayanthi
    Ehrenforth, Silke
    Hanabusa, Hideji
    Karim, Faraizah Abdul
    Kavakli, Kaan
    Khodaie, Melanie
    Staber, Janice
    Stasyshyn, Oleksandra
    Yee, Donald L.
    Rageliene, Lina
    [J]. THROMBOSIS AND HAEMOSTASIS, 2017, 117 (09) : 1705 - 1713
  • [10] Extended half-life pegylated, full-length recombinant factor VIII for prophylaxis in children with severe haemophilia A
    Mullins, E. S.
    Stasyshyn, O.
    Alvarez-Roman, M. T.
    Osman, D.
    Liesner, R.
    Engl, W.
    Sharkhawy, M.
    Abbuehl, B. E.
    [J]. HAEMOPHILIA, 2017, 23 (02) : 238 - 246