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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-9291861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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