Effect Of Food On The Pharmacokinetics Of Canagliflozin/Metformin (150/1,000 Mg) Immediate-Release Fixed-Dose Combination Tablet In Healthy Participants

Objective: To assess the effect of food on the pharmacokinetics (PK) of canagliflozin and metformin following administration of a canagliflozin/metformin (150/1,000 mg) immediate-release (IR) fixed-dose combination (FDC) tablet. Methods: A randomized, open-label, single-center, single-dose, 2-period, 2-sequence crossover study was conducted in healthy participants. Participants were randomized to 2 sequences of fasted and fed (or vice versa) administration of one 150/1,000 mg canagliflozin/metformin IR FDC, with 10 - 14 day washout between treatments. PK parameters (AUC, C-max, t(max), t(1/2)) were assessed for canagliflozin and metformin. Safety was evaluated. Results: When comparing the IRFDC tablet administered with and without food, PK parameters of canagliflozin were bioequivalent as the 90% confidence intervals (CIs) for log-transformed AUC(last), AUC(infinity), and C-max were within the bioequivalence limits of 80 - 125%. For metformin, overall exposure was similar under fed and fasted conditions as geometric mean ratios for AUC and associated 90% CI were contained within the bioequivalence limits, but geometric mean C-max decreased by 16% in the fed compared to fasted state. Both treatments were well tolerated with similar adverse events and most common were gastrointestinal events, generally attributed to metformin. Conclusions: Food did not affect canagliflozin bioavailability parameters (C-max and AUCs) or AUCs of metformin. The C-max of metformin was decreased by 16%, which is not considered clinically meaningful. The canagliflozin/metformin FDC tablet is recommended to be taken with meals to reduce the symptoms of gastrointestinal intolerability associated with metforrnin.