Effect of food on everolimus absorption: Quantification in healthy subjects and a confirmatory screening in patients with renal transplants

被引:68
作者
Kovarik, JM
Hartmann, S
Figueiredo, J
Rordorf, C
Golor, G
Lison, A
Budde, K
Neumayer, HH
机构
[1] Novartis Pharmaceut, Basel, Switzerland
[2] Parexel, Berlin, Germany
[3] Cent Hosp, Internal Med Clin, Bremen, Germany
[4] Univ Hosp Charite, Nephrol Sect, Berlin, Germany
来源
PHARMACOTHERAPY | 2002年 / 22卷 / 02期
关键词
D O I
10.1592/phco.22.3.154.33542
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Study Objective. To quantify the influence of a high-fat meal on the oral bioavailability of the immunosuppressant everolimus in a single-dose study in healthy subjects and to confirm the results in a small food-effect screening assessment in patients with renal transplants who were receiving multiple-dose everolimus. Design. Randomized, open-label, crossover, single-dose study and confirmatory screening. Setting. Phase 1 unit for the single-dose study and two German hospitals for the patient screening. Subjects. Twenty-four healthy male volunteers; six clinically stable patients with renal transplants who were originally part of a phase 1 dose-escalation study. Intervention. The 24 healthy men received everolimus 2 mg orally under fasting conditions and after a high-fat meal. The six patients received everolimus 2.5 mg/day orally, in addition to cyclosporine and prednisone. On two occasions, a pharmacokinetic profile was obtained over the dosing interval after drug administration under fasting conditions and after a high-fat meal in a randomized sequence. Measurements and Main Results. In the single-dose study in healthy subjects, a high-fat meal delayed everolimus time to maximum concentration (T-max) by a median 1.25 hours, reduced peak blood concentration (C-max) by 60%, and reduced area under the concentrationtime curve (AUC) by 16%. In the multiple-dose screening in patients with renal transplants, a high-fat meal delayed T-max by a median 1.75 hours and reduced C-max by 53% and AUC by 21%. Everolimus trough levels showed no food effect, whereas the peak-trough fluctuation was dampened by 52%. Conclusions. A high-fat meal modestly reduced everolimus AUC. To minimize longitudinal variability in exposure, everolimus should be administered consistently either with food or without food.
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收藏
页码:154 / 159
页数:6
相关论文
共 17 条
[1]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[2]   Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH [J].
Charman, WN ;
Porter, CJH ;
Mithani, S ;
Dressman, JB .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (03) :269-282
[3]   In vitro and in situ absorption of SDZ-RAD using a human intestinal cell line (Caco-2) and a single pass perfusion model in rats:: Comparison with rapamycin [J].
Crowe, A ;
Lemaire, M .
PHARMACEUTICAL RESEARCH, 1998, 15 (11) :1666-1672
[4]   Drug, meal and formulation interactions influencing drug absorption after oral administration - Clinical implications [J].
Fleisher, D ;
Li, C ;
Zhou, Y ;
Pao, LH ;
Karim, A .
CLINICAL PHARMACOKINETICS, 1999, 36 (03) :233-254
[5]   Longitudinal assessment of everolimus in de novo renal transplant recipients over the first post-transplant year: Pharmacokinetics, exposure-response relationships, and influence on cyclosporine [J].
Kovarik, JM ;
Kahan, BD ;
Kaplan, B ;
Lorber, M ;
Winkler, M ;
Rouilly, M ;
Gerbeau, C ;
Cambon, N ;
Boger, R ;
Rordorf, C .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (01) :48-56
[6]   INFLUENCE OF A FAT-RICH MEAL ON THE PHARMACOKINETICS OF A NEW ORAL FORMULATION OF CYCLOSPORINE IN A CROSSOVER COMPARISON WITH THE MARKET FORMULATIONS [J].
MUELLER, EA ;
KOVARIK, JM ;
VANBREE, JB ;
GREVEL, J ;
LUCKER, PW ;
KUTZ, K .
PHARMACEUTICAL RESEARCH, 1994, 11 (01) :151-155
[7]  
Neumayer HH, 1999, BRIT J CLIN PHARMACO, V48, P694
[8]   SDZ RAD, a new rapamycin derivative - Pharmacological properties in vitro and in vivo [J].
Schuler, W ;
Sedrani, R ;
Cottens, S ;
Haberlin, B ;
Schulz, M ;
Schuurman, HJ ;
Zenke, G ;
Zerwes, HG ;
Schreier, MH .
TRANSPLANTATION, 1997, 64 (01) :36-42
[9]   SDZ RAD, a new rapamycin derivative - Synergism with cyclosporine [J].
Schuurman, HJ ;
Cottens, S ;
Fuchs, S ;
Joergensen, J ;
Meerloo, T ;
Sedrani, R ;
Tanner, M ;
Zenke, G ;
Schuler, W .
TRANSPLANTATION, 1997, 64 (01) :32-35
[10]   Chemical modification of rapamycin: The discovery of SDZ RAD [J].
Sedrani, R ;
Cottens, S ;
Kallen, J ;
Schuler, W .
TRANSPLANTATION PROCEEDINGS, 1998, 30 (05) :2192-2194