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Pharmacokinetic comparison of sitagliptin and metformin HCl extended-release tablets versus JANUMET ® XR in healthy volunteers under fasting and fed conditions
Janumet XR is the combination of sitagliptin and extended metformin hydrochloride produced by Merck Sharp & Dohme. It is specially designed for diabetes mellitus patients taking both drugs already. Janumet XR exhibited clinically significant blood glucose lowering efficacy and long-term use safe...
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Published in: | Frontiers in pharmacology 2023-03, Vol.14, p.1105767-1105767 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Janumet
XR is the combination of sitagliptin and extended metformin hydrochloride produced by Merck Sharp & Dohme. It is specially designed for diabetes mellitus patients taking both drugs already. Janumet
XR exhibited clinically significant blood glucose lowering efficacy and long-term use safety. However, no generic form of Janumet
XR has been approved in western countries. The relatively high cost made the medication less prescribed. A more affordable form of this drug may benefit an immense diabetes mellitus population. The current study compared the bioequivalence (BE) of sitagliptin 100 mg and metformin 1000 mg produced by Nanjing Chia-Tai Tianqing Pharmaceutical Company to Janumet
XR in healthy Chinese subjects.
Twenty-eight healthy Chinese subjects were enrolled in Study 1 and 2, respectively. Both studies were conducted with an open, randomized, two-period crossover design using the test (T) or the reference (R) drug. Study 1 is conducted under the fasting state, and Study 2 is under the fed state. Subjects received an oral dose of sitagliptin 100 mg and metformin 1000 mg, and plasma concentrations of sitagliptin and metformin were determined up to 72 h post-dose. Pharmacokinetic (PK) parameters, including maximum serum concentration (C
) and area under the concentration-time curve up to the last quantifiable concentration (AUC
) of both sitagliptin and metformin, were calculated and compared between the T and R treatments.
In the fasting study, the geometric mean ratios of C
, AUC
, and AUC
for sitagliptin were 109.42%, 101.93%, and 101.95%, respectively; the corresponding ratios for metformin were 98.69%, 94.12%, and 93.42%, respectively. In the fed study, the geometric mean ratios of C
, AUC
, and AUC
for sitagliptin were 98.41%, 100.30%, and 100.24%, respectively; the corresponding ratios for metformin were 97.79%, 99.28%, and 100.69%, respectively. The 90% CIs of C
, AUC
, and AUC
in both studies were all within acceptance limits (80.00%-125.00%).
: The results demonstrated for the first time that sitagliptin 100 mg and metformin 1000 mg produced by Nanjing Chia-Tai Tianqing Pharmaceutical Company was bioequivalent to the branded Janumet
XR, and both drugs were well tolerated. |
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ISSN: | 1663-9812 1663-9812 |
DOI: | 10.3389/fphar.2023.1105767 |