The effect of morning versus evening administration of empagliflozin on its pharmacokinetics and pharmacodynamics characteristics in healthy adults: a two-way crossover, non-randomised trial.

: Empagliflozin is an SGLT2 inhibitor approved for use in patients with diabetes mellitus type 2 (DMT2) with or without other cardiovascular disease. Empagliflozin is taken once daily without rationale on the optimal timing for administration. This study aimed to determine the chronopharmacological effects of morning vs evening administration of empagliflozin (10 mg) in healthy Egyptian adults, by investigating the pharmacokinetics and pharmacodynamics parameters of empagliflozin depending on the intake time. An open label, sequential, two-way crossover trial comprised of two periods with a washout period of 7 days. All participants received a single oral dose of empagliflozin (JARDIANCE ®; 10 mg film coated tablet) in the evening, and after a seven-day washout period, the morning. Pharmacokinetics parameters (primary endpoints: t (h), C (ng/ml), AUC (ng.h/ml); secondary endpoints: AUC (ng.h/ml)) were assessed. Method validation was done prior to injection in LC/MS/MS and samples were processed by Liquid-Liquid extraction. The pharmacodynamic profile (UGE ) was determined after method validation (glucose hexokinase method). T increased by 35% in the evening phase compared to the morning phase, while C decreased by -6.5% in the evening dose compared to the morning dose. Additionally, AUC increased in the evening phase by 8.25% compared to the morning phase. The mean cumulative amount of glucose excreted (UGE ( )) increased by 43% in the evening dose compared to the morning dose : Despite the difference in pharmacokinetics parameters between evening and morning doses, C , AUC , AUC , didn't differ on the bioequivalence level. In addition, as UGE ( ) didn't statistically differ, thus, we can conclude that there is no statistical significance between the morning and evening doses. Clinal Trials.gov, ID: NCT03895229 (registered on 29 March 2019).