Int. Journal of Clinical Pharmacology and Therapeutics, Volume 55 (2017) - June (533 - 539)

Pharmacokinetic comparison using two tablets of an evogliptin/metformin XR 2.5/500 mg fixed dose combination vs. 1 tablet each of evogliptin 5 mg and metformin XR 1,000 mg

Sumin Yoon1, Su-jin Rhee1, Sang-In Park1, Seo Hyun Yoon1, Joo-Youn Cho1, In-Jin Jang1, SeungHwan Lee1,2, Kyung-Sang Yu1
1 Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, and 2 Clinical Trials Center, Seoul National University Biomedical Research Institute, Seoul, Republic of Korea

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DOI 10.5414/CP202930

Abstract

Objectives: The aim of this study was to compare the pharmacokinetic (PK) characteristics of evogliptin and metformin following the administration of 2 evogliptin/metformin extended-release (XR) 2.5/500 mg FDC tablets with the coadministration of separate evogliptin 5-mg and metformin XR 1,000-mg tablets (separate formulations). Methods: A randomized, two-period, two-sequence crossover study was conducted. Subjects were randomly assigned to receive 2 FDC tablets or the individual tablets, followed by a 14-day washout period and the administration of the alternate treatment. Blood samples were collected predose and up to 72 hours postdose for each period. PK parameters including Cmax and AUClast were calculated. The geometric mean ratios (GMRs) and the 90% confidence intervals (CIs) between FDC and the separate formulations were calculated for the Cmax and AUClast of evogliptin and metformin. Results: 33 subjects completed the study. The GMR (90% CI) values of Cmax and AUClast for evogliptin were 1.011 (0.959 – 1.066) and 1.010 (0.977 – 1.043), respectively. The GMR (90% CI) values of Cmax and AUClast for metformin were 0.892 (0.827 – 0.963) and 0.893 (0.841 – 0.947), respectively. There was no significant difference between the FDC and separate formulations regarding the occurrence of adverse events. All drug-related adverse events were considered to be mild and resolved without any treatment. Conclusions: Two FDC tablets of evogliptin/metformin XR 2.5/500 mg showed a similar PK profile to the separate formulations of evogliptin 5 mg and metformin XR 1,000 mg. All of the 90% CIs of GMR satisfied the regulatory bioequivalence criteria of 0.800 – 1.250.


Author Details

Authors

Departments

  • 1 Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, and
  • 2 Clinical Trials Center, Seoul National University Biomedical Research Institute, Seoul, Republic of Korea

Address

Kyung-Sang Yu, MD, PhD

Department of Clinical Pharmacology and Therapeutics
Seoul National University College of Medicine and Hospital
101 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea

Email: [email protected]

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Citation

Sumin Yoon, Su-jin Rhee, Sang-In Park, Seo Hyun Yoon, Joo-Youn Cho, In-Jin Jang, SeungHwan Lee, Kyung-Sang Yu.Pharmacokinetic comparison using two tablets of an evogliptin/metformin XR 2.5/500 mg fixed dose combination vs. 1 tablet each of evogliptin 5 mg and metformin XR 1,000 mg
. 2017; 55: 533-539. doi: 10.5414/CP202930.

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