A fixed-dose combination tablet of gemigliptin and metformin sustained release has comparable pharmacodynamic, pharmacokinetic, and tolerability profiles to separate tablets in healthy subjects

被引:7
作者
Park, Sang-In [1 ]
Lee, Howard [1 ,2 ]
Oh, Jaeseong [1 ]
Lim, Kyoung Soo [3 ,4 ]
Jang, In-Jin [1 ]
Kim, Jeong-Ae [5 ]
Jung, Jong Hyuk [5 ]
Yu, Kyung-Sang [1 ]
机构
[1] Seoul Natl Univ, Coll Med & Hosp, Dept Clin Pharmacol & Therapeut, Seoul 110799, South Korea
[2] Seoul Natl Univ, Clin Trials Ctr, Seoul Natl Univ Hosp, Dept Transdisciplinary Studies,Grad Sch Convergen, Seoul 110799, South Korea
[3] CHA Univ, Sch Med, Dept Clin Pharmacol & Therapeut, Songnam, South Korea
[4] CHA Bundang Med Ctr, Songnam, South Korea
[5] LG Life Sci Ltd, Seoul, South Korea
关键词
dipeptidyl peptidase 4; DPP-4; inhibitor; type 2 diabetes mellitus; T2DM; DOUBLE-BLIND; INHIBITOR; SITAGLIPTIN; EFFICACY; SAFETY; DRUG; MG;
D O I
10.2147/DDDT.S75980
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: In type 2 diabetes mellitus, fixed-dose combination (FDC) can provide the complementary benefits of correction of multiple pathophysiologic defects such as dysfunctions in glycemic or metabolic control while improving compliance compared with separate tablets taken together. The objective of the study reported here was to compare the pharmacodynamic (PD), pharmacokinetic (PK), and tolerability profiles of gemigliptin and extended-release metformin (metformin XR) between FDC and separate tablets. Methods: A randomized, open-label, single-dose, two-way, two-period, crossover study was conducted in 28 healthy male volunteers. Two FDC tablets of gemigliptin/metformin 25/500 mg or separate tablets of gemigliptin (50 mg x1) and metformin XR (500 mg x2) were orally administered in each period. Serial blood samples were collected up to 48 hours post-dose to determine dipeptidyl peptidase 4 (DPP-4) activity using spectrophotometric assay and concentrations of gemigliptin and metformin using tandem mass spectrometry. Geometric mean ratios (GMRs) of FDC to separate tablet formulations and their 90% confidence intervals (CIs) were calculated to compare the PD and PK parameters between the two formulations. Tolerability was assessed throughout the study. Results: The plasma DPP-4 activity-time curves of the FDC and the separate tablets almost overlapped, leading to a GMR (90% CI) of the FDC to separate tablets for the plasma DPP-4 activity and its maximum inhibition of 1.00 (0.97-1.04) and 0.92 (0.82-1.05), respectively. Likewise, all of the GMRs (90% CIs) of FDC to separate tablets for the area under the plasma concentration-time curve and maximum plasma concentration of gemigliptin and metformin fell entirely within the conventional bioequivalence range of 0.80-1.25. Both the FDC and separate tablets were well tolerated. Conclusion: The PD, PK, and tolerability profiles of gemigliptin and metformin XR in FDC and separate tablets were found to be comparable. The FDC tablet of gemigliptin and metformin sustained release can be a convenient therapeutic option in patients with type 2 diabetes mellitus requiring a combination approach.
引用
收藏
页码:729 / 736
页数:8
相关论文
共 14 条
[1]  
[Anonymous], GLUC METF HYDR TABL
[2]   Bioequivalence of Saxagliptin/Metformin Extended-Release (XR) Fixed-Dose Combination Tablets and Single-Component Saxagliptin and Metformin XR Tablets in Healthy Adult Subjects [J].
Boulton, David W. ;
Smith, Charles H. ;
Li, L. ;
Huang, Jian ;
Tang, Angela ;
LaCreta, Frank P. .
CLINICAL DRUG INVESTIGATION, 2011, 31 (09) :619-630
[3]  
Cefalu William T, 2007, JAAPA, VSuppl, P9
[4]   Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin added to ongoing metformin therapy in patients with type 2 diabetes inadequately controlled with metformin alone [J].
Charbonnel, Bernard ;
Karasik, Avraham ;
Liu, Ji ;
Wu, Mei ;
Meininger, Gary .
DIABETES CARE, 2006, 29 (12) :2638-2643
[5]   Effects of food on the pharmacokinetics of a gemigliptin/metformin sustained-release 50/1,000 mg (25/500 mg x 2 tablets) fixed-dose combination tablet in healthy male volunteers [J].
Choi, Hee Youn ;
Noh, Yook-Hwan ;
Kim, Yo Han ;
Kim, Mi Jo ;
Lee, Shi Hyang ;
Kim, Jeong-Ae ;
Kim, Bogyeong ;
Lim, Hyeong-Seok ;
Bae, Kyun-Seop .
INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2014, 52 (05) :381-391
[6]   Pharmacokinetics and dose proportionality of extended-release metformin following administration of 1000, 1500, 2000 and 2500 mg in healthy volunteers [J].
Cullen, E ;
Liao, J ;
Lukacsko, P ;
Niecestro, R ;
Friedhoff, L .
BIOPHARMACEUTICS & DRUG DISPOSITION, 2004, 25 (06) :261-263
[7]   From the Triumvirate to the Ominous Octet: A New Paradigm for the Treatment of Type 2 Diabetes Mellitus [J].
DeFronzo, Ralph A. .
DIABETES, 2009, 58 (04) :773-795
[8]   Gemigliptin, a novel dipeptidyl peptidase 4 inhibitor: first new anti-diabetic drug in the history of Korean pharmaceutical industry [J].
Kim, Sung-Ho ;
Lee, Sung-Hack ;
Yim, Hyeon-Joo .
ARCHIVES OF PHARMACAL RESEARCH, 2013, 36 (10) :1185-1188
[9]   Linagliptin/Metformin Fixed-Dose Combination Treatment: A Dual Attack to Type 2 Diabetes Pathophysiology [J].
Koliaki, Chrysi ;
Doupis, John .
ADVANCES IN THERAPY, 2012, 29 (12) :993-1004
[10]   Accelerating drug development using biomarkers: A case study with sitagliptin, a novel DPP4 inhibitor for type 2 diabetes [J].
Krishna, Rajesh ;
Herman, Gary ;
Wagner, John A. .
AAPS JOURNAL, 2008, 10 (02) :401-409