An individual bioequivalence approach to compare the intrasubject variability of two ciclosporin formulations, SangCya™, and Neoral®

被引:6
作者
Canafax, DM
Irish, WD
Moran, HB
Squiers, E
Levy, R
Pouletty, P
First, MR
Christians, U
机构
[1] Univ Calif San Francisco, Sch Pharm, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[2] Univ Cincinnati, Med Ctr, Cincinnati, OH 45267 USA
[3] SangSat Med Corp, Menlo Pk, CA USA
关键词
ciclosporin; pharmacokinetics; healthy volunteers; intraindividual variability; intrasubject variability; individual bioequivalence testing;
D O I
10.1159/000028307
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A novel bioequivalence testing approach was used to determine intrasubject variability and switchability of two ciclosporin formulations, SangCya(TM) (test) and Neoral(R) (reference). Twenty healthy volunteers were enrolled into a single-dose, randomized, open-label, 4-period, 2-sequence study with a crossover replicate design. Subject-by-formulation interaction variances were compared using a mixed effects linear model. Intrasubject variability for In AUC(0-infinity), and In C-max of SangCya and Neoral were not significantly different. The 95% confidence intervals of the intrasubject variability of AUC(0-infinity) (0.94) and C-max (1.28) as determined using the bootstrap nonparametric percentile method (n = 2,000) were below the individual bioequivalence limit estimated at 2.25. We concluded equivalent intrasubject variability of ciclosporin pharmacokinetics a nd switchability between SangCya and Neoral.
引用
收藏
页码:78 / 88
页数:11
相关论文
共 36 条
[21]   Clinical development of a cyclosporine microemulsion in transplantation [J].
Kovarik, JM ;
Mueller, EA ;
Niese, D .
THERAPEUTIC DRUG MONITORING, 1996, 18 (04) :429-434
[22]   PHARMACOKINETICS AND THERAPEUTIC DRUG-MONITORING OF IMMUNOSUPPRESSANTS [J].
LINDHOLM, A ;
SAWE, J .
THERAPEUTIC DRUG MONITORING, 1995, 17 (06) :570-573
[23]   USE OF THE REPEATED CROSS-OVER DESIGNS IN ASSESSING BIOEQUIVALENCE [J].
LIU, JP .
STATISTICS IN MEDICINE, 1995, 14 (9-10) :1067-1078
[24]   Role of intestinal P-glycoprotein (mdr1) in interpatient variation in the oral bioavailability of cyclosporine [J].
Lown, KS ;
Mayo, RR ;
Leichtman, AB ;
Hsiao, HL ;
Turgeon, DK ;
SchmiedlinRen, P ;
Brown, MB ;
Guo, WS ;
Rossi, SJ ;
Benet, LZ ;
Watkins, PB .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1997, 62 (03) :248-260
[25]  
*MED EC CO, 1998, PHYS DESK REF, P1882
[26]   Individual and average bioequivalence of highly variable drugs and drug products [J].
Midha, KK ;
Rawson, MJ ;
Hubbard, JW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (11) :1193-1197
[27]   CYCLOSPORINE - A REVIEW OF THE PHARMACOKINETIC PROPERTIES, CLINICAL EFFICACY AND TOLERABILITY OF A MICROEMULSION-BASED FORMULATION (NEORAL) [J].
NOBLE, S ;
MARKHAM, A .
DRUGS, 1995, 50 (05) :924-941
[28]  
OHAHSHI Y, 1996, BIOAVAILABILITY BIOE, P113
[29]   Switching between cyclosporin formulations - What are the risks? [J].
Olyaei, AJ ;
deMattos, AM ;
Bennett, WM .
DRUG SAFETY, 1997, 16 (06) :366-373
[30]   Individual bioequivalence - New concepts in the statistical assessment of bioequivalence metrics [J].
Patnaik, RN ;
Lesko, LJ ;
Chen, ML ;
Wiliams, RL ;
Balch, A ;
Chan, K ;
Machado, S ;
Schuirmann, D ;
Hauck, W ;
Schall, R .
CLINICAL PHARMACOKINETICS, 1997, 33 (01) :1-6