Preclinical safety and efficacy of a new recombinant FIX drug product for treatment of hemophilia B

被引:18
作者
Dietrich, Barbara [1 ]
Schiviz, Alexandra [1 ]
Hoellriegl, Werner [1 ]
Horling, Frank [1 ]
Benamara, Karima [1 ]
Rottensteiner, Hanspeter [1 ]
Turecek, Peter L. [1 ]
Schwarz, Hans Peter [1 ]
Scheiflinger, Friedrich [1 ]
Muchitsch, Eva-Maria [1 ]
机构
[1] Baxter Innovat GmbH, A-1221 Vienna, Austria
关键词
Hemophilia B; rFIX; Pharmacokinetics; Safety; Efficacy; FACTOR-IX; MODERATELY SEVERE; PROPHYLAXIS; PROTEIN; BLOOD;
D O I
10.1007/s12185-013-1448-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Baxter has developed a new recombinant factor IX (rFIX) drug product (BAX326) for treating patients with hemophilia B, or congenital FIX deficiency. An extensive preclinical program evaluated the pharmacokinetics, efficacy, and safety of BAX326 in different species. The efficacy of BAX326 was tested in three mouse models of primary pharmacodynamics: tail-tip bleeding, carotid occlusion, and thrombelastography. The pharmacokinetics was evaluated after a single intravenous bolus injection in mice, rats, and macaques. Toxicity was assessed in rats and macaques, safety pharmacology in rabbits and macaques, and immunogenicity in mice. BAX326 was shown to be efficacious in all three primary pharmacodynamic studies (P a parts per thousand currency sign 0.0076). Hemostatic efficacy was dose related and similar for the three lots tested. Pharmacokinetic results showed that rFIX activity and rFIX antigen concentrations declined in a bi-phasic manner, similar to a previously licensed rFIX product. BAX326 was well tolerated in rabbits and macaques at all dose levels; no thrombogenic events and no adverse clinical, respiratory, or cardiovascular effects occurred. BAX326 was also shown to have a similar immunogenicity profile to the comparator rFIX product in mice. These results demonstrate that BAX326 has a favorable preclinical safety and efficacy profile, predictive of a comparable effect to that of the previously licensed rFIX in humans.
引用
收藏
页码:525 / 532
页数:8
相关论文
共 21 条
[1]   Overview of inhibitors [J].
Astermark, Jan .
SEMINARS IN HEMATOLOGY, 2006, 43 (02) :S3-S7
[2]   HUMAN PARVOVIRUS INFECTION IN HEMOPHILIACS 1ST INFUSED WITH TREATED CLOTTING FACTOR CONCENTRATES [J].
CORSI, OB ;
AZZI, A ;
MORFINI, M ;
FANCI, R ;
ROSSIFERRINI, P .
JOURNAL OF MEDICAL VIROLOGY, 1988, 25 (02) :165-170
[3]   Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B [J].
Bicocchi, MP ;
Pasino, M ;
Rosano, C ;
Molinari, AC ;
Della Valle, E ;
Lanza, T ;
Bottini, F ;
Acquila, M .
HAEMOPHILIA, 2006, 12 (03) :263-270
[4]   Recombinant human factor IX: Replacement therapy, prophylaxis, and pharmacokinetics in canine hemophilia B [J].
Brinkhous, KM ;
Sigman, JL ;
Read, MS ;
Stewart, PF ;
McCarthy, KP ;
Timony, GA ;
Leppanen, SD ;
Rup, BJ ;
Keith, JC ;
Garzone, PD ;
Schaub, RG .
BLOOD, 1996, 88 (07) :2603-2610
[5]   Murine thrombosis models [J].
Day, SM ;
Reeve, JL ;
Myers, DD ;
Fay, WP .
THROMBOSIS AND HAEMOSTASIS, 2004, 92 (03) :486-494
[6]   Haemophilia B: database of point mutations and short additions and deletions - eighth edition [J].
Giannelli, F ;
Green, PM ;
Sommer, SS ;
Poon, MC ;
Ludwig, M ;
Schwaab, A ;
Reitsma, PH ;
Goossens, M ;
Yoshioka, A ;
Figueiredo, MS ;
Brownlee, GG .
NUCLEIC ACIDS RESEARCH, 1998, 26 (01) :265-268
[7]  
GRAY E, 1995, THROMB HAEMOSTASIS, V73, P675
[8]  
Jesmok G, 2006, BLOOD, V11, P108
[9]  
Jesmok G, 2007, J THROMB HAEMOST, V5, pP
[10]   Prophylaxis in factor IX deficiency product and patient variation [J].
Kisker, CT ;
Eisberg, A ;
Schwartz, B .
HAEMOPHILIA, 2003, 9 (03) :279-284