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. 2021 Nov;10(11):1297-1306.
doi: 10.1002/cpdd.970. Epub 2021 Jul 2.

Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations

Affiliations

Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations

Daryl J Fediuk et al. Clin Pharmacol Drug Dev. 2021 Nov.

Abstract

Ertugliflozin, a sodium-glucose cotransporter 2 inhibitor, is approved for treatment of type 2 diabetes. Two population pharmacokinetic (PK) analyses were conducted, using data from up to 17 phase 1 to 3 studies, to characterize ertugliflozin PK parameters in select ethnic subgroups: (1) East/Southeast (E/SE) Asian vs non-E/SE Asian subjects; (2) Asian subjects from mainland China vs Asian subjects from the rest of the world and non-Asian subjects. A 2-compartment model with first-order absorption, lag time, and first-order elimination was fitted to the observed data. For the E/SE Asian vs non-E/SE Asian analysis (13 692 PK observations from 2276 subjects), E/SE Asian subjects exhibited a 17% increase in apparent clearance (CL/F) and 148% increase in apparent central volume of distribution (Vc/F) vs non-E/SE Asian subjects. However, individual post hoc CL/F values were similar between groups when body weight differences were considered. For the second analysis (16 018 PK observations from 2620 subjects), compared with non-Asian subjects, CL/F was similar while Vc/F increased by 44% in Asian subjects from mainland China and both CL/F and Vc/F increased in Asian subjects from the rest of the world (8% and 115%, respectively) vs non-Asian subjects. Increases in Vc/F would decrease the ertugliflozin maximum concentration but would not impact area under the concentration-time curve. Therefore, the differences in CL/F (area under the concentration-time curve) and Vc/F were not considered clinically relevant or likely to result in meaningful ethnic differences in the PK of ertugliflozin.

Trial registration: ClinicalTrials.gov NCT00989079 NCT01127308 NCT01054300 NCT01223339 NCT01948986 NCT01096667 NCT01059825 NCT01986855 NCT02033889 NCT02099110 NCT01958671 NCT02630706.

Keywords: diabetes; ertugliflozin; population pharmacokinetics; sodium-glucose cotransporter 2 inhibitor.

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Conflict of interest statement

D.J.F., V.S., V.K.D., and K.S. are employees of Pfizer Inc., New York, NY, USA and may own shares/stock options in Pfizer Inc. S.Z. is an employee of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA and may own stock in Merck & Co., Inc., Kenilworth, NJ, USA.

Figures

Figure 1
Figure 1
Final model individual post hoc apparent clearance (CL/F) for E/SE Asian and non‐E/SE Asian subjects. Boxes provide median and 25th and 75th percentiles, and the lower/upper whiskers extend to 1.5× the interquartile range. Data points beyond the end of the whiskers are outliers. CL/F, individual post hoc apparent clearance; E/SE, East/Southeast.
Figure 2
Figure 2
Final model individual post hoc apparent clearance (CL/F) for non‐Asian subjects, Asian subjects from mainland China, and Asian subjects from the rest of the world. Boxes provide median and 25th and 75th percentiles, and the lower/upper whiskers extend to 1.5× the interquartile range. Data points beyond the end of the whiskers are outliers. CL/F, individual post hoc apparent clearance; ROW, rest of the world.

References

    1. International Diabetes Federation . IDF Diabetes Atlas, 9th ed. Brussels, Belgium. https://www.diabetesatlas.org. Published 2019. Accessed December 18, 2020.
    1. Abdul‐Ghani MA, Norton L, DeFronzo RA. Renal sodium‐glucose cotransporter inhibition in the management of type 2 diabetes mellitus. Am J Physiol Renal Physiol. 2015;309(11):F889‐F900. - PMC - PubMed
    1. Kalgutkar AS, Tugnait M, Zhu T, et al. Preclinical species and human disposition of PF‐04971729, a selective inhibitor of the sodium‐dependent glucose cotransporter 2 and clinical candidate for the treatment of type 2 diabetes mellitus. Drug Metab Dispos. 2011;39(9):1609‐1619. - PubMed
    1. Miao Z, Nucci G, Amin N, et al. Pharmacokinetics, metabolism, and excretion of the antidiabetic agent ertugliflozin (PF‐04971729) in healthy male subjects. Drug Metab Dispos. 2013;41(2):445‐456. - PubMed
    1. Dagogo‐Jack S, Liu J, Eldor R, et al. Efficacy and safety of the addition of ertugliflozin in patients with type 2 diabetes mellitus inadequately controlled with metformin and sitagliptin: The VERTIS SITA2 placebo‐controlled randomized study. Diabetes Obes Metab. 2018;20(3):530‐540. - PMC - PubMed

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