Pharmacokinetics of etoricoxib in patients with renal impairment

被引:18
作者
Agrawal, NGB
Matthews, CZ
Mazenko, RS
Kline, WE
Woolf, EJ
Porras, AG
Geer, LA
Wong, PH
Cho, MH
Cote, J
Marbury, TC
Moncrief, JW
Alcorn, H
Swan, S
Sack, MR
Robson, RA
Petty, KJ
Schwartz, JI
Gottesdiener, KM
机构
[1] Merck Res Labs, Dept Drug Metab, W Point, PA 19486 USA
[2] Merck Res Labs, Rahway, NJ USA
[3] Merck Res Labs, Blue Bell, PA USA
[4] Orlando Clin Res Ctr, Orlando, FL USA
[5] PPD Dev Inc, Austin, TX USA
[6] Total Renal Res Inc, Minneapolis, MN USA
[7] Radiant Res Austin, Austin, TX USA
[8] Christchurch Clin Studies Trust, Christchurch, New Zealand
关键词
etoricoxib; pharmacokinetics; renal impairment; bioavailability; cyclooxygenase; COX-2;
D O I
10.1177/0091270003260338
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenose-2,as examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m(2)], 5 severe [creatinine clearance below 30 2 mL/min/1.73 m(2)], and 6 with end-stage renal disease requiring hemodialysis) following administration of single 120-mg oral doses of etoricoxib. Even the most severe renal impairment was found to have little effect on etoricoxib pharmacokinetics. The low recovery of etoricoxib in dialysate (less than 6% of the dose) supports that hemodialysis also has little effect on etoricoxib pharmacokinetics, and binding of etoricoxib to plasma proteins was generally unaffected by renal disease. Single doses of etoricoxib were generally well tolerated by patients with renal impairment. Based on pharmacokinetic considerations, dosing adjustments are not necessary for patients with any degree of renal impairment. However, because patients with advanced renal disease (creatinine clearance below 30 mL/min/1.73 m(2)) are likely to be very sensitive to any further compromise of renal function, and there is no long-term clinical experience in these patients, the use of etoricoxib is not recommended in patients with advanced renal disease.
引用
收藏
页码:48 / 58
页数:11
相关论文
共 21 条
[1]
Single- and multiple-dose pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase-2, in man [J].
Agrawal, NGB ;
Porras, AG ;
Matthews, CZ ;
Rose, MJ ;
Woolf, EJ ;
Musser, BJ ;
Dynder, AL ;
Mazina, KE ;
Lasseter, KC ;
Hunt, TL ;
Schwartz, JI ;
McCrea, JB ;
Gottesdiener, KM .
JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 43 (03) :268-276
[2]
Dose proportionality of oral etoricoxib, a highly selective cyclooxygenase-2 inhibitor, in healthy volunteers [J].
Agrawal, NGB ;
Porras, AG ;
Matthews, CZ ;
Woolf, EJ ;
Miller, JL ;
Mukhopadhyay, S ;
Neu, DC ;
Gottesdiener, KM .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (10) :1106-1110
[3]
Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. [J].
Bombardier, C ;
Laine, L ;
Reicin, A ;
Shapiro, D ;
Burgos-Vargas, R ;
Davis, B ;
Day, R ;
Ferraz, MB ;
Hawkey, CJ ;
Hochberg, MC ;
Kvien, TK ;
Schnitzer, TJ ;
Weaver, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (21) :1520-1528
[4]
Renal effects of COX-2-selective inhibitors [J].
Brater, DC ;
Harris, C ;
Redfern, JS ;
Gertz, BJ .
AMERICAN JOURNAL OF NEPHROLOGY, 2001, 21 (01) :1-15
[5]
In vitro metabolism considerations, including activity testing of metabolites, in the discovery and selection of the COX-2 inhibitor etoricoxib (MK-0663) [J].
Chauret, N ;
Yergey, JA ;
Brideau, C ;
Friesen, RW ;
Mancini, J ;
Riendeau, D ;
Silva, J ;
Styhler, A ;
Trimble, LA ;
Nicoll-Griffith, DA .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (08) :1059-1062
[6]
PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[7]
Review article: COX-II inhibitors - A new generation of safer NSAIDs? [J].
Donnelly, MT ;
Hawkey, CJ .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1997, 11 (02) :227-236
[8]
A comparison of adverse renovascular experiences among osteoarthritis patients treated with rofecoxib and comparator non-selective non-steroidal anti-inflammatory agents [J].
Gertz, BJ ;
Krupa, D ;
Bolognese, JA ;
Sperling, RS ;
Reicin, A .
CURRENT MEDICAL RESEARCH AND OPINION, 2002, 18 (02) :82-91
[9]
Results of a randomized, dose-ranging trial of etoricoxib in patients with osteoarthritis [J].
Gottesdiener, K ;
Schnitzer, T ;
Fisher, C ;
Bockow, B ;
Markenson, J ;
Ko, A ;
DeTora, L ;
Curtis, S ;
Geissler, L ;
Gertz, BJ .
RHEUMATOLOGY, 2002, 41 (09) :1052-1061
[10]
Cyclo-oxygenase isoenzymes - How recent findings affect thinking about nonsteroidal anti-inflammatory drugs [J].
Jouzeau, JY ;
Terlain, B ;
Abid, A ;
Nedelec, E ;
Netter, P .
DRUGS, 1997, 53 (04) :563-582