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Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations

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/Southe...

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Autores principales: Fediuk, Daryl J., Sahasrabudhe, Vaishali, Dawra, Vikas Kumar, Zhou, Susan, Sweeney, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291861/
https://www.ncbi.nlm.nih.gov/pubmed/34213819
http://dx.doi.org/10.1002/cpdd.970
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author Fediuk, Daryl J.
Sahasrabudhe, Vaishali
Dawra, Vikas Kumar
Zhou, Susan
Sweeney, Kevin
author_facet Fediuk, Daryl J.
Sahasrabudhe, Vaishali
Dawra, Vikas Kumar
Zhou, Susan
Sweeney, Kevin
author_sort Fediuk, Daryl J.
collection PubMed
description 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.
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spelling pubmed-92918612022-07-20 Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations Fediuk, Daryl J. Sahasrabudhe, Vaishali Dawra, Vikas Kumar Zhou, Susan Sweeney, Kevin Clin Pharmacol Drug Dev Articles 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. John Wiley and Sons Inc. 2021-07-02 2021-11 /pmc/articles/PMC9291861/ /pubmed/34213819 http://dx.doi.org/10.1002/cpdd.970 Text en © 2021 Merck Sharp & Dohme Corp and Pifzer Inc. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Fediuk, Daryl J.
Sahasrabudhe, Vaishali
Dawra, Vikas Kumar
Zhou, Susan
Sweeney, Kevin
Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations
title Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations
title_full Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations
title_fullStr Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations
title_full_unstemmed Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations
title_short Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations
title_sort population pharmacokinetic analyses of ertugliflozin in select ethnic populations
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291861/
https://www.ncbi.nlm.nih.gov/pubmed/34213819
http://dx.doi.org/10.1002/cpdd.970
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