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
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