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Antimicrobial Agents and Chemotherapy, February 2007, p. 495-502, Vol. 51, No. 2
0066-4804/07/$08.00+0 doi:10.1128/AAC.00472-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Schering-Plough Research Institute, Kenilworth, New Jersey,1 Research Solutions, Little Rock, Arkansas,2 Covance GFI Research, Evansville, Indiana3
Received 17 April 2006/ Returned for modification 30 August 2006/ Accepted 31 October 2006
Posaconazole is a triazole antifungal for prophylaxis of invasive fungal infection and treatment of oropharyngeal candidiasis. We evaluated the effects of gender, age, and race/ethnicity (black or white) on the steady-state pharmacokinetics of posaconazole in two studies on healthy adult subjects (
18 years of age). Additionally, we explored the effect of P-glycoprotein expression and MDR1 genotype on posaconazole pharmacokinetics in black and white subjects. Age, gender, and race/ethnicity had no clinically relevant effects on posaconazole pharmacokinetics. No association was observed between any MDR1 single-nucleotide polymorphism and the area under the concentration-time curve for posaconazole. Posaconazole was safe and well tolerated regardless of age, gender, or race/ethnicity. In conclusion, age, gender, and race/ethnicity have no clinically relevant effects on the steady-state pharmacokinetics of posaconazole in healthy adults; therefore, dosage adjustments based on these covariates are unnecessary.
Published ahead of print on 13 November 2006.
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