Single and multiple dose pharmacokinetics of rifapentine in man: part II.
Int J Tuberc Lung Dis
; 3(5): 437-44, 1999 May.
Article
em En
| MEDLINE
| ID: mdl-10331734
ABSTRACT
OBJECTIVE:
To characterize the pharmacokinetics of rifapentine following single, multiple, and intermittent doses.DESIGN:
Twenty-three healthy male volunteers were randomized in a two-period, incomplete block, crossover design to receive two of four possible treatments single daily oral rifapentine doses of 150, 300, or 600 mg given on day 1 and again on days 4-10, or a single oral 600 mg dose given on days 1, 4, 7, and 10.RESULTS:
Maximum rifapentine plasma concentrations were observed in 4-5 hours. Mean rifapentine t(1/2) ranged from 13.2-14.1 hours and was similar across the 150-600 mg dose range. The changes in rifapentine Cmax (R = 0.86) and AUC(0-->infinity) (R + 0.90) were dose linear. The active 25-desacetyl metabolite appeared slowly in plasma, with mean Tmax of 14.4-17.8 hours. Mean t(1/2) for 25-desacetyl-rifapentine ranged from 13.3-24.3 hours. Disproportionate, dose-dependent increases in rifapentine and 25-desacetyl-rifapentine AUC were observed as single doses of rifapentine increased from 150 to 600 mg. At steady state, however, the magnitude of dose dependency was much less.CONCLUSION:
Maximum plasma rifapentine concentrations were well above minimum inhibitory concentrations for Mycobacterium tuberculosis and M. avium following single 600 mg doses. In addition, the extended t(1/2) of rifapentine and its active metabolite support clinical investigation of once or twice-weekly rifapentine dosage regimens of rifapentine for the management of tuberculosis.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Rifampina
/
Antituberculosos
Tipo de estudo:
Clinical_trials
Limite:
Adult
/
Humans
/
Male
Idioma:
En
Revista:
Int J Tuberc Lung Dis
Ano de publicação:
1999
Tipo de documento:
Article
País de afiliação:
Estados Unidos