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J Clin Pharmacol ; 46(2): 193-200, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16432271

RESUMO

An open-label, nonrandomized study was conducted to assess the effect of ravuconazole on the pharmacokinetics of concomitantly administered nelfinavir. Healthy volunteers received 750 mg nelfinavir on day 1, 750 mg nelfinavir and 400 mg ravuconazole on day 2, 400 mg ravuconazole on days 3 to 28, and 750 mg nelfinavir and 400 mg ravuconazole on day 29. The geometric means of C(max) and area under the curve of nelfinavir coadministered with ravuconazole were 30.7% and 31.9% higher on day 2 and 7.9% and 16.2% lower on day 29, respectively, compared to the corresponding values on day 1. These findings are consistent with the potential for ravuconazole to both inhibit and induce CYP3A isozymes. The alterations in the systemic exposure to nelfinavir were within the range defined by the 90% confidence interval. The study data indicate that coadministration of ravuconazole did not result in a clinically significant change in the plasma levels of nelfinavir.


Assuntos
Fármacos Anti-HIV/farmacocinética , Nelfinavir/farmacocinética , Tiazóis/farmacologia , Triazóis/farmacologia , Adolescente , Adulto , Fármacos Anti-HIV/efeitos adversos , Área Sob a Curva , Citocromo P-450 CYP3A/metabolismo , Interações Medicamentosas , Meia-Vida , Humanos , Masculino , Pessoa de Meia-Idade , Nelfinavir/efeitos adversos , Tiazóis/efeitos adversos , Triazóis/efeitos adversos
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