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http://dx.doi.org/10.4333/KPS.2004.34.5.413

Bioequivalence of MelaxTM Capsule to MobicTM Capsule (Meloxicam 7.5 mg)  

Lee, Ye-Rie (Department of Drug Development Service, BioCore Co., Ltd.)
Yeom, Seung-Bock (Department of Drug Development Service, BioCore Co., Ltd.)
Ko, Youn-Jung (Department of Drug Development Service, BioCore Co., Ltd.)
Ko, Jung-Kil (Department of Drug Development Service, BioCore Co., Ltd.)
Kim, Ho-Hyun (Department of Drug Development Service, BioCore Co., Ltd., Department of Pharmacokinetics, Seoul Medical Science Institute, Seoul Clinical Laboratories)
Lee, Hee-Joo (Department of Drug Development Service, BioCore Co., Ltd., Department of Pharmacokinetics, Seoul Medical Science Institute, Seoul Clinical Laboratories)
Lee, Kyung-Ryul (Department of Drug Development Service, BioCore Co., Ltd., Department of Pharmacokinetics, Seoul Medical Science Institute, Seoul Clinical Laboratories)
Publication Information
Journal of Pharmaceutical Investigation / v.34, no.5, 2004 , pp. 413-418 More about this Journal
Abstract
A bioequivalence of $Melax^{TM}$ capsules (Chong Kun Dang Pharm., Korea) and $Mobic^{TM}$ capsules (Boehringer Ingelheim Korea) was evaluated according to the guideline of Korea Food and Drug Administration (KFDA). Single 15 mg dose of meloxicam of each medicine was administered orally to 24 healthy male volunteers. This study was performed in a $2\;{\times}\;2$ crossover design. Concentrations of meloxicam in human plasma were monitored by a high-performance liquid chromatography. $AUC_t$ (the area under the plasma concentration-time curve from time zero to 72 hr) was calculated by the linear trapezoidal rule method. $C_{max}$ (maximum plasma drug concentration) and $T_{max}$ (time to reach $C_{max}$) were compiled from the plasma concentration-time data. Analysis of variance was performed using logarithmically transformed $AUC_t$ and $C_{max}$. No significant sequence effect was found for all of the bioavailability parameters. The 90% confidence intervals of the $AUC_t$ ratio and the $C_{max}$ ratio for $Melax^{TM}/Mobic^{TM}$ were 0.95 - 1.04 and 0.98 - 1.14, respectively. This study demonstrated a bioequivalence of $Melax^{TM}$ and $Mobic^{TM}$ with respect to the rate and extent of absorption.
Keywords
Meloxicam; $Melax^{TM}$; $Mobic^{TM}$; Bioequvalence; HPLC;
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  • Reference
1 S. Noble and J. Balfour, Meloxicam, Drug, 51(3), 424-430 (1996)   DOI   ScienceOn
2 N.M. Davies and N.M. Skjodi, Clinical Pharmacokinetics of Meloxicam, A Cyclooxygenase-2 Preferential Nonsteroidal Anti-Inflammatory Drug. Clinical Pharmacokinetics, 36(2), 115-126 (1999)   DOI   ScienceOn
3 Effect of Food on the Pharmacokinetics of Meloxicam after Oral Administration, Pharmacokinetics, 9(5), 270-276 (1995)
4 식품의약품안전청 고시 제 2002-60호, 생물학적동등성시험기준 (2002. 11. 22)
5 Y.J. Lee, Y.G. Kim, M.G. Lee, S.J. Chung, M.H. Lee and C.K. Shim, Analysis of bioequivalence study using logtransformed model. Yakhakhoeji, 44, 308-314 (2000)
6 식품의약품안전청 고시 제 2002-61호, 의약품동등성시험관리규정 (2002.11.22)