Evidence map›Paper›PMID 40424011›Full record

ReviewClinical pharmacology and therapeutics2025

Predicting OCT2/MATEs-Mediated Drug Interactions in Healthy Volunteers and Patients with Chronic Kidney Disease: Insights from Extended Clearance Concept, Endogenous Biomarkers, and In Vitro Inhibition Studies (Perspectives from the International Transporter Consortium).

Satoshi Asano, Aleksandra Galetin, Yoshiko Tomita, Kathleen M Giacomini, Xiaoyan Chu, Xinning Yang, Toshimichi Nakamura, Hiroyuki Kusuhara, Yuichi Sugiyama

Abstract readReview
In one paragraph

Review in Clinical pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Gut microbes · 2026
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  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Satoshi AsanoTranslational Research Division, Chugai Pharmaceutical Co., Ltd., Kanagawa, Japan.ORCID 0000-0002-8489-2960
Aleksandra GaletinCentre for Applied Pharmacokinetic Research, University of Manchester, Manchester, UK.ORCID 0000-0002-3933-5217
Yoshiko TomitaClinical Research, Drug Development Division, Sumitomo Pharma Co., Ltd., Osaka, Japan.ORCID 0000-0001-5422-792X
Kathleen M GiacominiDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0001-8041-5430
Xiaoyan ChuDepartment of Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB), Merck & Co., Inc., Rahway, New Jersey, USA.ORCID 0000-0001-7223-9000
Xinning YangOffice of Clinical Pharmacology, US Food and Drug Administration, Silver Spring, Maryland, USA.ORCID 0000-0002-8689-8231
Toshimichi NakamuraNon-Clinical Biomedical Science, Applied Research & Operations, Astellas Pharma Inc., Ibaraki, Japan.ORCID 0000-0003-2766-7203
Hiroyuki KusuharaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Yuichi SugiyamaLaboratory of Quantitative System Pharmacokinetics/Pharmacodynamics, Innovation Base, Josai International University, Tokyo, Japan.ORCID 0000-0002-8452-8835

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organic cation transporter (OCT) 2 and multidrug and toxin extrusion (MATE) transporters play significant roles in the renal secretion of organic cations and drug-drug interactions (DDIs). Recent in vitro studies indicate that the K

Indexed as

Organic Cation Transporter 2Organic Cation Transport ProteinsRenal Insufficiency, ChronicBiomarkersDrug InteractionsHealthy VolunteersHumansKidneyMetabolic Clearance RateModels, BiologicalBiomarkersOrganic Cation Transporter 2Organic Cation Transport ProteinsSLC22A2 protein, human

Identifiers

PMID40424011
PMCPMC12598135

What OpenQuestion holds

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Registered trials

None linked

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 OpenQuestion graph.