Pharmacokinetics in renally impaired subjects of NXY-059, a nitrone-based, free-radical trapping agent developed for the treatment of acute stroke

被引:24
作者
Strid, S [1 ]
Borgå, O
Edenius, C
Jostell, KG
Odergren, T
Weil, A
机构
[1] AstraZeneca R&D Sodertalje, S-15185 Sodertalje, Sweden
[2] APEX Res GMBH, D-81241 Munich, Germany
[3] Borga PK Konsult HB, S-21116 Malmo, Sweden
[4] Biolipox AB, S-10234 Stockholm, Sweden
关键词
renal impairment; pharmacokinetics; dosage regimens;
D O I
10.1007/s00228-002-0478-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: N-XY-059 is a nitrone-based, free-radical trapping agent being developed for the treatment of acute ischaemic stroke. Elimination of NXY-059 is primarily renal. The objective of the study was to investigate the pharmacokinetics of N-XY-059 in subjects with renal impairment. Methods: Twenty-four subjects with a glomerular filtration rate (GFR) ranging from 19 ml/min to 100 ml/min received NXY-059 intravenously over a 24-h period. Drug in plasma and urine was measured for 72 h. One-hour loading infusion rates were proportional to body weight, while maintenance infusion rates were proportional to GFR. Target plasma levels were 60 mumol/l for subjects with mild (GFR 50-100 ml/min) and moderate (GFR 30-49 ml/min) renal impairment, and 30 mumol/l for subjects with severe renal impairment (GFR < 30 ml/min). GFR was measured as sinistrin clearance. Results: The data indicated no tolerability or safety concerns with NXY-059. The half-life, which normally is approximately 2-4 h, was in the order of 10-12 h in subjects with moderate and severe renal impairment. The distribution parameters steady-state volume of distribution (V-ss) and unbound fraction in plasma at 13-151 and 0.53-0.58, respectively, were virtually the same as previously observed in healthy subjects. Plasma clearance of NXY-059, which ranged from 9 ml/min to 76 ml/min, was directly proportional to kidney function (GFR) with no discernible contribution by non-renal clearance. The correlation coefficient squared (r(2)) was 0.93, both when the renal function parameter was GFR and when it was creatinine clearance estimated from serum creatinine, age, weight and sex. Conclusion: Non-renal elimination of NXY-059 appeared to be insignificant even in subjects with low renal capacity. Patients with renal impairment should have their dose of NXY-059 adjusted for renal function, conveniently assessed from serum creatinine.
引用
收藏
页码:409 / 415
页数:7
相关论文
共 11 条
[1]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[2]  
DETTLI L, 1976, Clinical Pharmacokinetics, V1, P126, DOI 10.2165/00003088-197601020-00004
[3]  
Edenius Charlotte, 2002, J Stroke Cerebrovasc Dis, V11, P34, DOI 10.1053/jscd.2002.123973
[4]  
Food and Drug Administration, 1998, GUID IND PHARM PAT I
[5]  
*FRES PHARM AUSTR, SCI BROCH IN
[6]   Neuroprotective effects of a novel nitrone, NXY-059, after transient focal cerebral ischemia in the rat [J].
Kuroda, S ;
Tsuchidate, R ;
Smith, ML ;
Maples, KR ;
Siesjö, BK .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (07) :778-787
[7]   Tolerability and pharmacokinetics of the nitrone NXY-059 in patients with acute stroke [J].
Lees, KR ;
Sharma, AK ;
Barer, D ;
Ford, GA ;
Kostulas, V ;
Cheng, YF ;
Odergren, T .
STROKE, 2001, 32 (03) :675-680
[8]   NXY-059, a free radical-trapping agent, substantially lessens the functional disability resulting from cerebral ischemia in a primate species [J].
Marshall, JWB ;
Duffin, KJ ;
Green, AR ;
Ridley, RR .
STROKE, 2001, 32 (01) :190-197
[9]   REASSESSMENT OF THE SINGLE INTRAVENOUS-INJECTION METHOD WITH INULIN FOR MEASUREMENT OF THE GLOMERULAR-FILTRATION RATE IN MAN [J].
PRESCOTT, LF ;
FREESTONE, S ;
MCAUSLANE, JAN .
CLINICAL SCIENCE, 1991, 80 (02) :167-176
[10]   PROTEIN BINDING OF DIPHENYLHYDANTOIN AND DESMETHYLIMIPRAMINE IN PLASMA FROM PATIENTS WITH POOR RENAL FUNCTION [J].
REIDENBERG, MM ;
ODARCEDE.I ;
BAHR, CV ;
BORGA, O ;
SJOQVIST, F .
NEW ENGLAND JOURNAL OF MEDICINE, 1971, 285 (05) :264-+