Pharmacokinetics of Etoricoxib in Patients with Renal Impairment

The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/mi...

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Veröffentlicht in:Journal of clinical pharmacology 2004-01, Vol.44 (1), p.48-58
Hauptverfasser: Agrawal, Nancy G. B., Matthews, Catherine Z., Mazenko, Ralph S., Kline, Walter F., Woolf, Eric J., Porras, Arturo G., Geer, Leslie A., Wong, Peggy H., Cho, Meehung, Cote, Josee, Marbury, Thomas C., Moncrief, Jack W., Alcorn Jr, Harry, Swan, Suzanne, Sack, Marshall R., Robson, Richard A., Petty, Kevin J., Schwartz, Jules I., Gottesdiener, Keith M.
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container_issue 1
container_start_page 48
container_title Journal of clinical pharmacology
container_volume 44
creator Agrawal, Nancy G. B.
Matthews, Catherine Z.
Mazenko, Ralph S.
Kline, Walter F.
Woolf, Eric J.
Porras, Arturo G.
Geer, Leslie A.
Wong, Peggy H.
Cho, Meehung
Cote, Josee
Marbury, Thomas C.
Moncrief, Jack W.
Alcorn Jr, Harry
Swan, Suzanne
Sack, Marshall R.
Robson, Richard A.
Petty, Kevin J.
Schwartz, Jules I.
Gottesdiener, Keith M.
description The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/min/1.73 m2], 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 m2) 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.
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B. ; Matthews, Catherine Z. ; Mazenko, Ralph S. ; Kline, Walter F. ; Woolf, Eric J. ; Porras, Arturo G. ; Geer, Leslie A. ; Wong, Peggy H. ; Cho, Meehung ; Cote, Josee ; Marbury, Thomas C. ; Moncrief, Jack W. ; Alcorn Jr, Harry ; Swan, Suzanne ; Sack, Marshall R. ; Robson, Richard A. ; Petty, Kevin J. ; Schwartz, Jules I. ; Gottesdiener, Keith M.</creator><creatorcontrib>Agrawal, Nancy G. 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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 m2) 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.</description><identifier>ISSN: 0091-2700</identifier><identifier>EISSN: 1552-4604</identifier><identifier>DOI: 10.1177/0091270003260338</identifier><identifier>PMID: 14681341</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Adult ; Aged ; Area Under Curve ; bioavailability ; Biological Availability ; Clinical Trials as Topic ; COX-2 ; cyclooxygenase ; Cyclooxygenase Inhibitors - pharmacokinetics ; Etoricoxib ; Female ; Half-Life ; Humans ; Kidney Failure, Chronic - metabolism ; Kidney Failure, Chronic - therapy ; Male ; Metabolic Clearance Rate ; Middle Aged ; pharmacokinetics ; Protein Binding ; Pyridines - pharmacokinetics ; Renal Dialysis ; renal impairment ; Sulfones - pharmacokinetics</subject><ispartof>Journal of clinical pharmacology, 2004-01, Vol.44 (1), p.48-58</ispartof><rights>2004 American College of Clinical Pharmacology</rights><rights>2004 SAGE Publications</rights><rights>Copyright SAGE PUBLICATIONS, INC. 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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. 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B.</au><au>Matthews, Catherine Z.</au><au>Mazenko, Ralph S.</au><au>Kline, Walter F.</au><au>Woolf, Eric J.</au><au>Porras, Arturo G.</au><au>Geer, Leslie A.</au><au>Wong, Peggy H.</au><au>Cho, Meehung</au><au>Cote, Josee</au><au>Marbury, Thomas C.</au><au>Moncrief, Jack W.</au><au>Alcorn Jr, Harry</au><au>Swan, Suzanne</au><au>Sack, Marshall R.</au><au>Robson, Richard A.</au><au>Petty, Kevin J.</au><au>Schwartz, Jules I.</au><au>Gottesdiener, Keith M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics of Etoricoxib in Patients with Renal Impairment</atitle><jtitle>Journal of clinical pharmacology</jtitle><addtitle>J Clin Pharmacol</addtitle><date>2004-01</date><risdate>2004</risdate><volume>44</volume><issue>1</issue><spage>48</spage><epage>58</epage><pages>48-58</pages><issn>0091-2700</issn><eissn>1552-4604</eissn><abstract>The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/min/1.73 m2], and 6 with end‐stage renal disease requiring hemodialysis) following administration of single 120‐mg oral doses of etoricoxib. 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However, because patients with advanced renal disease (creatinine clearance below 30 mL/min/1.73 m2) 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.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>14681341</pmid><doi>10.1177/0091270003260338</doi><tpages>11</tpages></addata></record>
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subjects Administration, Oral
Adult
Aged
Area Under Curve
bioavailability
Biological Availability
Clinical Trials as Topic
COX-2
cyclooxygenase
Cyclooxygenase Inhibitors - pharmacokinetics
Etoricoxib
Female
Half-Life
Humans
Kidney Failure, Chronic - metabolism
Kidney Failure, Chronic - therapy
Male
Metabolic Clearance Rate
Middle Aged
pharmacokinetics
Protein Binding
Pyridines - pharmacokinetics
Renal Dialysis
renal impairment
Sulfones - pharmacokinetics
title Pharmacokinetics of Etoricoxib in Patients with Renal Impairment
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