Literature DB >> 16509761

Effects of chronic renal failure on the pharmacokinetics of ruboxistaurin and its active metabolite 338522.

Stephen Wise1, Eunice Yuen, Clark Chan, Yeo Kwee Poo, Lorraine Teng, Titus Lau, James Voelker.   

Abstract

BACKGROUND: Ruboxistaurin, a specific inhibitor of the beta(1) and beta(2) isoforms of protein kinase C, is currently in clinical development for the treatment of several diabetic microvascular complications. The major metabolite, N-desmethyl ruboxistaurin (metabolite 338522), is equipotent in its inhibitory activity. The elimination of ruboxistaurin and its metabolites is primarily through bile and the faecal route, with urinary excretion constituting only a minor route.
OBJECTIVE: To assess the effects of chronic renal insufficiency on the pharmacokinetics of ruboxistaurin and metabolite 338522.
METHODS: Six healthy subjects (creatinine clearance >80 mL/min/1.73 m(2)) and six end-stage renal disease (ESRD) subjects requiring long-term haemodialysis were studied. All subjects received a single oral dose of ruboxistaurin 32 mg followed by serial blood sampling up to 72 hours. ESRD subjects underwent haemodialysis approximately 58 hours after dosing, with blood samples obtained immediately before and after dialysis.
RESULTS: No differences were observed in the pharmacokinetic parameters (area under the plasma concentration-time curve from time zero to infinity [AUC(infinity)], maximum plasma concentration [C(max)] and elimination half-life [t(1/2)]) of ruboxistaurin and metabolite 338522 between healthy and ESRD subjects Plasma concentrations of ruboxistaurin were below the lower limit of quantification by the time of haemodialysis. The predicted post-dialysis plasma concentrations of metabolite 338522 were not statistically different from the observed values (p=0.163). Ruboxistaurin was well tolerated in both groups of subjects.
CONCLUSION: These results indicate that the kidney is not an important route of metabolism or excretion for ruboxistaurin and metabolite 338522. Based on the pharmacokinetic and tolerability findings, no formal dosage adjustment of ruboxistaurin should be required for patients with any degree of renal impairment who are undergoing haemodialysis.

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Year:  2006        PMID: 16509761     DOI: 10.2165/00003088-200645030-00005

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  15 in total

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2.  Prediction of creatinine clearance from serum creatinine.

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4.  Elevated glucose promotes generation of endothelium-derived vasoconstrictor prostanoids in rabbit aorta.

Authors:  B Tesfamariam; M L Brown; D Deykin; R A Cohen
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5.  Vascular endothelial growth factor-induced retinal permeability is mediated by protein kinase C in vivo and suppressed by an orally effective beta-isoform-selective inhibitor.

Authors:  L P Aiello; S E Bursell; A Clermont; E Duh; H Ishii; C Takagi; F Mori; T A Ciulla; K Ways; M Jirousek; L E Smith; G L King
Journal:  Diabetes       Date:  1997-09       Impact factor: 9.461

6.  (S)-13-[(dimethylamino)methyl]-10,11,14,15-tetrahydro-4,9:16, 21-dimetheno-1H, 13H-dibenzo[e,k]pyrrolo[3,4-h][1,4,13]oxadiazacyclohexadecene-1,3(2H)-d ione (LY333531) and related analogues: isozyme selective inhibitors of protein kinase C beta.

Authors:  M R Jirousek; J R Gillig; C M Gonzalez; W F Heath; J H McDonald; D A Neel; C J Rito; U Singh; L E Stramm; A Melikian-Badalian; M Baevsky; L M Ballas; S E Hall; L L Winneroski; M M Faul
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7.  The interactions of a selective protein kinase C beta inhibitor with the human cytochromes P450.

Authors:  Barbara J Ring; Jennifer S Gillespie; Shelly N Binkley; Kristina M Campanale; Steven A Wrighton
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8.  Preferential elevation of protein kinase C isoform beta II and diacylglycerol levels in the aorta and heart of diabetic rats: differential reversibility to glycemic control by islet cell transplantation.

Authors:  T Inoguchi; R Battan; E Handler; J R Sportsman; W Heath; G L King
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Review 9.  A novel potential therapy for diabetic nephropathy and vascular complications: protein kinase C beta inhibition.

Authors:  Katherine R Tuttle; Pamela W Anderson
Journal:  Am J Kidney Dis       Date:  2003-09       Impact factor: 8.860

10.  Amelioration of vascular dysfunctions in diabetic rats by an oral PKC beta inhibitor.

Authors:  H Ishii; M R Jirousek; D Koya; C Takagi; P Xia; A Clermont; S E Bursell; T S Kern; L M Ballas; W F Heath; L E Stramm; E P Feener; G L King
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  1 in total

1.  Inhibition of PKCα/β with ruboxistaurin antagonizes heart failure in pigs after myocardial infarction injury.

Authors:  Dennis Ladage; Lisa Tilemann; Kiyotake Ishikawa; Robert N Correll; Yoshiaki Kawase; Steven R Houser; Jeffery D Molkentin; Roger J Hajjar
Journal:  Circ Res       Date:  2011-10-13       Impact factor: 17.367

  1 in total

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