Evidence mapPaperPMID 34213819Full record

ArticleClinical pharmacology in drug development2021

Population Pharmacokinetic Analyses of Ertugliflozin in Select Ethnic Populations.

Daryl J Fediuk, Vaishali Sahasrabudhe, Vikas Kumar Dawra, Susan Zhou, Kevin Sweeney

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In one paragraph

Article in Clinical pharmacology in drug development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
field-weighted citation impact, top 88% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Daryl J FediukPfizer, Inc., Groton, Connecticut, USA.
Vaishali SahasrabudhePfizer, Inc., Groton, Connecticut, USA.
Vikas Kumar DawraPfizer, Inc., New York, New York, USA.
Susan ZhouMerck & Co., Inc., Kenilworth, New Jersey, USA.
Kevin SweeneyPfizer, Inc., Groton, Connecticut, USA.
Pfizer (United States) · USMerck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Asian PeopleAdultAgedAsia, EasternAsia, SoutheasternBridged Bicyclo Compounds, HeterocyclicChinaDiabetes Mellitus, Type 2EthnicityFemaleHumansMaleMiddle AgedSodium-Glucose Transporter 2 InhibitorsBridged Bicyclo Compounds, HeterocyclicertugliflozinSodium-Glucose Transporter 2 Inhibitorsdiabetesertugliflozinpopulation pharmacokineticssodium-glucose cotransporter 2 inhibitor

Identifiers

PMID34213819
PMCPMC9291861
OpenAlexW3175207923

What Socratic holds

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.