Evidence map›Paper›PMID 31628668›Full record

Trial reportClinical pharmacology and therapeutics2020

Dose-Dependent Inhibition of OATP1B by Rifampicin in Healthy Volunteers: Comprehensive Evaluation of Candidate Biomarkers and OATP1B Probe Drugs.

Daiki Mori, Emi Kimoto, Brian Rago, Yusuke Kondo, Amanda King-Ahmad, Ragu Ramanathan, Linda S Wood, Jillian G Johnson, Vu H Le, Manoli Vourvahis and 5 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 102 citations in OpenAlex.

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  16. Conjugated hyperbilirubinemia associated with accidental rifapentine overdose.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2024
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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

15 authors at 4 institutions in 2 countries.

Daiki MoriLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Emi KimotoADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Brian RagoADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Yusuke KondoLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Amanda King-AhmadADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Ragu RamanathanADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Linda S WoodClinical Pharmacogenomics Lab, Early Clinical Development, Pfizer Inc., Groton, Connecticut, USA.
Jillian G JohnsonClinical Pharmacogenomics Lab, Early Clinical Development, Pfizer Inc., Groton, Connecticut, USA.
Vu H LeBiostatistics, Pfizer Inc., Collegeville, PA, USA.
Manoli VourvahisClinical Pharmacology, Pfizer Inc., New York, New York, USA.
A David RodriguesADME Sciences, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.
Chieko MutoPfizer Inc., Tokyo, Japan.
Kenichi FurihataP-One Clinic, Keikokai Medical Corp, Tokyo, Japan.
Yuichi SugiyamaRIKEN Innovation Center, Research Cluster for Innovation, RIKEN, 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) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To address the most appropriate endogenous biomarker for drug-drug interaction risk assessment, eight healthy subjects received an organic anion transporting polypeptide 1B (OATP1B) inhibitor (rifampicin, 150, 300, and 600 mg), and a probe drug cocktail (atorvastatin, pitavastatin, rosuvastatin, and valsartan). In addition to coproporphyrin I, a widely studied OATP1B biomarker, we identified at least 4 out of 28 compounds (direct bilirubin, glycochenodeoxycholate-3-glucuronide, glycochenodeoxycholate-3-sulfate, and hexadecanedioate) that presented good sensitivity and dynamic range in terms of the rifampicin dose-dependent change in area under the plasma concentration-time curve ratio (AUCR). Their suitability as OATP1B biomarkers was also supported by the good correlation of AUC

Indexed as

AdultAntibiotics, AntitubercularBiomarkersCross-Over StudiesDose-Response Relationship, DrugDrug EvaluationDrug InteractionsHealthy VolunteersHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLiver-Specific Organic Anion Transporter 1MaleRifampinAntibiotics, AntitubercularBiomarkersHydroxymethylglutaryl-CoA Reductase InhibitorsLiver-Specific Organic Anion Transporter 1RifampinSLCO1B1 protein, human

Identifiers

PMID31628668
PMCPMC7158214
OpenAlexW2981070774

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.