Oral bioavailability of posaconazole in fasted healthy subjects - Comparison between three regimens and basis for clinical dosage recommendations

被引:142
作者
Ezzet, F [1 ]
Wexler, D [1 ]
Courtney, R [1 ]
Krishna, G [1 ]
Lim, J [1 ]
Laughlin, M [1 ]
机构
[1] Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA
关键词
D O I
10.2165/00003088-200544020-00006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and objective: Posaconazole is a potent, extended- spectrum triazole antifungal agent currently in clinical development for the treatment of invasive fungal infections. This study was conducted to compare the bioavailability and resulting serum concentrations of posaconazole 800mg following administration of three different dose regimens to fasting adults. Study design: This was a randomised, open-label, three-way crossover study. Methods: Subjects fasted 12 hours before and 48 hours after the administration of posaconazole oral suspension (800mg) given as a single dose (regimen A), 400mg every 12 hours (regimen 13) or 200mg every 6 hours (regimen Q. Plasma posaconazole concentrations were determined for 48 hours after the initial dose and subjects completed a 1-week washout period between treatment regimens. A one-compartment oral model with first-order rate of absorption and first-order rate of elimination was fitted to the plasma concentration-time data. Differences in exposure were investigated by allowing the biclavailability fraction to vary among regimens. Study participants: A total of 18 healthy men were enrolled in and completed the study. Main outcome measures and results: Posaconazole relative bioavailability was estimated to be significantly different among regimens (p < 0.0001) and increased with the number of doses, such that regimen B/regimen A = 1.98 +/- 0.35, representing a 98% increase, and regimen C/regimen A = 3.20 +/- 0.69, or a 220% increase. With use of the one-compartment model, the population steady-state values for area under the concentration-time curve over 24 hours were predicted to be 3900, 7700 and 12 400 mug (.) h/L, with average plasma concentrations of 162, 320 and 517 mug/L for regimens A, B and C, respectively. Conclusion: These data suggest that divided daily dose administration (every 12 or 6 hours) significantly increases posaconazole exposure under fasted conditions.
引用
收藏
页码:211 / 220
页数:10
相关论文
共 28 条
  • [1] ARIKAN S, 2000, EMERGING DRUGS, V5, P135
  • [2] In vitro and in vivo activities of SCH 56592 (posaconazole), a new triazole antifungal agent, against Aspergillus and Candida
    Cacciapuoti, A
    Loebenberg, D
    Corcoran, E
    Menzel, F
    Moss, EL
    Norris, C
    Michalski, M
    Raynor, K
    Halpern, J
    Mendrick, C
    Arnold, B
    Antonacci, B
    Parmegiani, R
    Yarosh-Tomaine, T
    Miller, GH
    Hare, RS
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (08) : 2017 - 2022
  • [3] In vitro activities of four novel triazoles against Scedosporium spp.
    Carrillo, AJ
    Guarro, J
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (07) : 2151 - 2153
  • [4] Treatment strategies for Aspergillus infections
    Chiller, TM
    Stevens, DA
    [J]. DRUG RESISTANCE UPDATES, 2000, 3 (02) : 89 - 97
  • [5] Comparison of a new triazole, posaconazole, with itraconazole and amphotericin B for treatment of histoplasmosis following pulmonary challenge in immunocompromised mice
    Connolly, P
    Wheat, LJ
    Schnizlein-Bick, C
    Durkin, M
    Kohler, S
    Smedema, M
    Goldberg, J
    Brizendine, E
    Loebenberg, D
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (10) : 2604 - 2608
  • [6] Effect of food on the relative bioavailability of two oral formulations of posaconazole in healthy adults
    Courtney, R
    Wexler, D
    Radwanski, E
    Lim, J
    Laughlin, M
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 57 (02) : 218 - 222
  • [7] Pharmacokinetics, safety, and tolerability of oral posaconazole administered in single and multiple doses in healthy adults
    Courtney, R
    Pai, S
    Laughlin, M
    Lim, J
    Batra, V
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) : 2788 - 2795
  • [8] In vitro susceptibilities of zygomycetes to conventional and new antifungals
    Dannaoui, E
    Meletiadis, J
    Mouton, JW
    Meis, JFGM
    Verweij, PE
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (01) : 45 - 52
  • [9] EZZET F, 2001, INT C ANT AG CHEM 20
  • [10] Identification of dematiaceous fungi and their role in human disease
    Fothergill, AW
    [J]. CLINICAL INFECTIOUS DISEASES, 1996, 22 : S179 - S184