Drug-drug interaction study between a novel oral ibandronate formulation and metformin

被引:0
|
作者
Bittner, Beate [1 ]
McIntyre, Christine [1 ]
Jordan, Paul [2 ]
Schmidt, Johannes [3 ]
机构
[1] F Hoffmann La Roche Ltd, Clin Pharmacol, Basel, Switzerland
[2] F Hoffmann La Roche Ltd, Biostat, Basel, Switzerland
[3] F Hoffmann La Roche Ltd, Pharma Med Global Prod Strategy, Basel, Switzerland
来源
ARZNEIMITTEL-FORSCHUNG-DRUG RESEARCH | 2011年 / 61卷 / 12期
关键词
Drug-drug interaction; Ibandronate; Metformin; SNAC; HUMAN GROWTH-HORMONE; POSTMENOPAUSAL OSTEOPOROSIS; INTESTINAL-ABSORPTION; SODIUM; DELIVERY; HEPARIN; MOBILE; AGENTS;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The novel excipient, sodium N-[8-(2-hydroxybenzoyl)amino]caprylate (SNAC, CAS 203787-91-1) increases the oral bioavailability of co-formulated ibandronate (IBN, CAS 138926-19). The aim of this study was to investigate the effect of the IBN/SNAC formulation on the steady-state pharmacokinetics of metformin (CAS 657-24-9) and to assess safety and tolerability of IBN/SNAC when dosed in combination with metformin. Twenty-two healthy subjects received metformin on Days 1 to 6. On Day 7, subjects received metformin together with the IBN/SNAG formulation. The safety and tolerability of IBN/SNAC co-administered with metformin was consistent with the known safety profile of the single medications. The increase in mean maximum plasma concentration (C(max)) and mean overall exposure to metformin (AUC(0-t)) was approximately 7%. The entire 90% confidence intervals for the AUC- and C(max)-ratios did fall within the acceptance region for bioequivalence (0.8-1.25). In summary, administration of the IBN/SNAG formulation together with metformin did not lead to a significant increase in exposure to metformin. The study medication was well tolerated in healthy volunteers.
引用
收藏
页码:707 / 713
页数:7
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