Evidence map›Paper›PMID 35421902›Full record

ArticleClinical and translational science2022

Physiologically-based pharmacokinetic model-based translation of OATP1B-mediated drug-drug interactions from coproporphyrin I to probe drugs.

Tatsuki Mochizuki, Yasunori Aoki, Takashi Yoshikado, Kenta Yoshida, Yurong Lai, Hideki Hirabayashi, Yoshiyuki Yamaura, Kevin Rockich, Kunal Taskar, Tadayuki Takashima and 7 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

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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

17 authors at 14 institutions in 3 countries.

Tatsuki MochizukiLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Yasunori AokiLaboratory of Quantitative System Pharmacokinetics/Pharmacodynamics, School of Pharmacy, Josai International University, Tokyo, Japan.
Takashi YoshikadoLaboratory of Clinical Pharmacology, Yokohama University of Pharmacy, Yokohama, Kanagawa, Japan.
Kenta YoshidaClinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.ORCID 0000-0003-4967-3831
Yurong LaiDrug Metabolism, Gilead Sciences Inc., Foster City, California, USA.ORCID 0000-0001-9505-333X
Hideki HirabayashiDrug Metabolism and Pharmacokinetics Research Laboratories, Research, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Yoshiyuki YamauraPharmacokinetic Research Laboratories, Ono Pharmaceutical Co., Ltd., Osaka, Japan.
Kevin RockichDrug Metabolism, Pharmacokinetics, and Clinical Pharmacology, Incyte Research Institute, Wilmington, Delaware, USA.
Kunal TaskarDrug Metabolism and Pharmacokinetics, IVIVT, GlaxoSmithKline, Stevenage, UK.
Tadayuki TakashimaLaboratory for Safety Assessment & ADME, Pharmaceuticals Research Center, Asahi Kasei Pharma Corporation, Shizuoka, Japan.
Xiaoyan ChuDepartment of Pharmacokinetics, Pharmacodynamics & Drug Metabolism, Merck & Co., Inc., Kenilworth, New Jersey, USA.
Maciej J Zamek-GliszczynskiDrug Metabolism and Disposition, GlaxoSmithKline, Collegeville, Pennsylvania, USA.
Jialin MaoDrug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, California, USA.
Kazuya MaedaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-9174-5213
Kenichi FurihataP-One Clinic, Keikokai Medical Corp, Tokyo, Japan.
Yuichi SugiyamaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Hiroyuki KusuharaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
The University of Tokyo · JPJosai International University · JPAsahi Kasei (Japan) · JPGenentechGilead Sciences (United Kingdom) · GBGlaxoSmithKline (United Kingdom) · GBGlaxoSmithKline (United States) · USIncyte (United States) · USKishokai Medical Corporation · JPMerck & Co., Inc., Rahway, NJ, USA (United States) · USOno Pharmaceutical (Japan) · JPSunesis (United States) · USTakeda (Japan) · JPYokohama University of Pharmacy · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The accurate prediction of OATP1B-mediated drug-drug interactions (DDIs) is challenging for drug development. Here, we report a physiologically-based pharmacokinetic (PBPK) model analysis for clinical DDI data generated in heathy subjects who received oral doses of cyclosporin A (CysA; 20 and 75 mg) as an OATP1B inhibitor, and the probe drugs (pitavastatin, rosuvastatin, and valsartan). PBPK models of CysA and probe compounds were combined assuming inhibition of hepatic uptake of endogenous coproporphyrin I (CP-I) by CysA. In vivo K

Indexed as

CoproporphyrinsModels, BiologicalDrug InteractionsHumansLiver-Specific Organic Anion Transporter 1Rosuvastatin Calciumcoproporphyrin ICoproporphyrinsLiver-Specific Organic Anion Transporter 1Rosuvastatin Calcium

Identifiers

PMID35421902
PMCPMC9199885
OpenAlexW4224015281

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.