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J Clin Pharmacol ; 45(12): 1368-72, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16291711

ABSTRACT

Eighteen adult subjects with mild to moderate hepatic impairment and 18 healthy control subjects were given a single 15-mg dose of sirolimus by oral solution. Mean whole-blood sirolimus weight-normalized oral-dose clearances (CL/F) were significantly decreased (P = .02) in subjects with mild to moderate hepatic impairment by -31.8% and -36.0%, respectively, compared with controls. There were no significant differences in mean sirolimus C(max) and t(max) values among groups. The observed decreases in CL/F may be relevant in renal transplant patients with mild to moderate hepatic impairment, based on the close similarity of sirolimus CL/F in controls and previously studied stable renal transplant patients receiving multiple-dose administration of sirolimus and cyclosporine. There was considerable overlap in the CL/F values of hepatic-impaired subjects and controls, suggesting that whole-blood sirolimus trough concentrations in renal transplant patients exhibiting mild to moderate hepatic impairment be initially monitored to assess the need for dose adjustments.


Subject(s)
Immunosuppressive Agents/pharmacokinetics , Liver Diseases/metabolism , Sirolimus/pharmacokinetics , Adult , Female , Humans , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/blood , Kidney Transplantation , Liver Diseases/blood , Male , Metabolic Clearance Rate , Sirolimus/adverse effects , Sirolimus/blood
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