Evidence map›Paper›PMID 32866300›Full record

Trial reportClinical pharmacology and therapeutics2021

Identification of Appropriate Endogenous Biomarker for Risk Assessment of Multidrug and Toxin Extrusion Protein-Mediated Drug-Drug Interactions in Healthy Volunteers.

Takeshi Miyake, Emi Kimoto, Lina Luo, Sumathy Mathialagan, Lauren M Horlbogen, Ragu Ramanathan, Linda S Wood, Jillian G Johnson, Vu H Le, Manoli Vourvahis and 5 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% of its field
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Article
  7. IsMetabolites · 2025
    Article
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  17. Transporters in Regulatory Science: Notable Contributions from Dr. Giacomini in the Past Two Decades.Drug metabolism and disposition: the biological fate of chemicals · 2022
    Article
  18. Pharmaceutics · 2021
    Article
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

15 authors at 5 institutions in 2 countries.

Takeshi MiyakeLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Emi KimotoADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Lina LuoADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Sumathy MathialaganADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Lauren M HorlbogenADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Ragu RamanathanADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Linda S WoodClinical Pharmacogenomics Laboratory, Early Clinical Development, Pfizer Inc, Groton, Connecticut, USA.
Jillian G JohnsonClinical Pharmacogenomics Laboratory, Early Clinical Development, Pfizer Inc, Groton, Connecticut, USA.
Vu H LeBiostatics, Pfizer Inc., Collegeville, Pennsylvania, USA.
Manoli VourvahisClinical Pharmacology, Pfizer Inc., New York, New York, USA.
A David RodriguesADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Chieko MutoClinical Pharmacology, Pfizer R&D Japan, Tokyo, Japan.
Kenichi FurihataP-One Clinic, Keikokai Medical Corp, Tokyo, Japan.
Yuichi SugiyamaSugiyama Laboratory, RIKEN Baton Zone Program, RIKEN Cluster for Science, Technology and Innovation Hub, RIKEN, Yokohama, Kanagawa, Japan.
Hiroyuki KusuharaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Pfizer (United States) · USThe University of Tokyo · JPKishokai Medical Corporation · JPPfizer (Japan) · JPRIKEN Center for Sustainable Resource Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endogenous biomarkers are emerging to advance clinical drug-drug interaction (DDI) risk assessment in drug development. Twelve healthy subjects received a multidrug and toxin exclusion protein (MATE) inhibitor (pyrimethamine, 10, 25, and 75 mg) in a crossover fashion to identify an appropriate endogenous biomarker to assess MATE1/2-K-mediated DDI in the kidneys. Metformin (500 mg) was also given as reference probe drug for MATE1/2-K. In addition to the previously reported endogenous biomarker candidates (creatinine and N

Indexed as

AdultAsian PeopleBiomarkersCell LineCreatinineCross-Over StudiesDrug InteractionsHealthy VolunteersHEK293 CellsHumansHypoglycemic AgentsKidneyMaleMetforminOrganic Cation Transport ProteinsPyrimethamineBiomarkersCreatinineHypoglycemic AgentsMetforminOrganic Cation Transport ProteinsPyrimethamine

Identifiers

PMID32866300
PMCPMC7891601
OpenAlexW3082877508

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.