Archive/Bioequivalence Evaluation of Immediate-Release Empagliflozin/Metformin Fixed-Dose Combination Tablets Under Fed Conditions in Healthy Mexican Subjects and Exploratory Analysis of Metformin Dose Proportionality
Bioequivalence Evaluation of Immediate-Release Empagliflozin/Metformin Fixed-Dose Combination Tablets Under Fed Conditions in Healthy Mexican Subjects and Exploratory Analysis of Metformin Dose Proportionality
Erika Gabriela Guido Ávila, Alberto Martínez Muñoz, Porfirio de la Cruz Cruz et al.
31 de julio de 2026
en

Abstract

Background/Objectives: Fixed-dose combinations (FDCs) improve therapeutic adherence in type 2 diabetes. These studies aimed to evaluate the pharmacokinetics and establish the bioequivalence of four immediate-release empagliflozin/metformin FDC formulations under fed conditions in healthy Mexican subjects. Methods: A total of 42 healthy volunteers per study (168 total) were enrolled in four randomized, open-label, two-way crossover, single-dose studies with a 14-day washout period. Formulations were administered orally under standardized fed conditions. Plasma concentrations of both drugs were quantified using a validated liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) method. Results: Across all dose strengths, the 90% confidence intervals (CIs) for the geometric mean ratios of peak plasma concentration (Cmax) and area under the concentration–time curve (AUC0-t) for both empagliflozin and metformin were entirely within the 80.00–125.00% bioequivalence acceptance range. The specific 90% CIs for Cmax and AUC0-t were: Study A (5/850 mg): empagliflozin (90.18–103.16%; 94.37–101.81%), metformin (98.43–107.69%; 97.18–106.62%); Study B (12.5/500 mg): empagliflozin (91.94–102.77%; 93.38–98.51%), metformin (92.58–101.73%; 94.85–103.91%); Study C (12.5/850 mg): empagliflozin (95.47–107.74%; 95.34–101.25%), metformin (94.19–103.59%; 94.06–103.21%); and Study D (12.5/1000 mg): empagliflozin (94.53–107.10%; 98.13–105.66%), metformin (98.89–107.51%; 99.25–109.92%). Regarding safety, no serious adverse events occurred, and all reported events were mild or moderate and resolved completely. Conclusions: All evaluated empagliflozin/metformin FDCs successfully demonstrated bioequivalence and a favorable safety profile under fed conditions. These findings fulfill regulatory requirements and support their therapeutic interchangeability in clinical practice. An exploratory power-model analysis indicated a modest trend toward less-than-dose-proportional metformin exposure across the 500–1000 mg range (slope β ≈ 0.77–0.78). NCT07633015, NCT07633054, NCT07633028, and NCT07633041.

IPC Classification

A61H01

Keywords

bioequivalenceevaluationimmediate-releaseempagliflozinmetforminfixed-dosecombinationtabletsconditionshealthymexicansubjectsexploratoryanalysisdoseproportionalitypharmaceuticalsbackgroundobjectivescombinationsfdcsimprovetherapeuticadherence
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