Evidence map›Paper›PMID 37561322›Full record

ArticlePharmaceutical research2023

Utilization of Rosuvastatin and Endogenous Biomarkers in Evaluating the Impact of Ritlecitinib on BCRP, OATP1B1, and OAT3 Transporter Activity.

Yeamin Huh, Anna Plotka, Hua Wei, Julia Kaplan, Nancy Raha, Justin Towner, Vivek S Purohit, Martin E Dowty, Robert Wolk, Manoli Vourvahis and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Pharmaceutical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
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

16 authors at 2 institutions in 2 countries.

Yeamin HuhPfizer Inc, Groton, CT, USA. YeaMin.Huh@pfizer.com.ORCID http://orcid.org/0000-0003-0365-4467
Anna PlotkaPfizer Inc, Collegeville, PA, USA.
Hua WeiPfizer Inc, Shanghai, China.
Julia KaplanPfizer Inc, Groton, CT, USA.
Nancy RahaPfizer Inc, Groton, CT, USA.
Justin TownerPfizer Inc, Groton, CT, USA.
Vivek S PurohitPfizer Inc, Groton, CT, USA.
Martin E DowtyPfizer Inc, Cambridge, MA, USA.
Robert WolkPfizer Inc, Groton, CT, USA.
Manoli VourvahisPfizer Inc, New York, NY, USA.
Amanda King-AhmadPfizer Inc, Groton, CT, USA.
Sumathy MathialaganPfizer Inc, Groton, CT, USA.
Mark A WestPfizer Inc, Groton, CT, USA.
Sarah LazzaroPfizer Inc, Groton, CT, USA.
Sangwoo RyuPfizer Inc, Groton, CT, USA.
A David RodriguesPfizer Inc, Groton, CT, USA.
Pfizer (United States) · USPfizer (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRitlecitinib, an inhibitor of Janus kinase 3 and tyrosine kinase expressed in hepatocellular carcinoma family kinases, is in development for inflammatory diseases. This study assessed the impact of ritlecitinib on drug transporters using a probe drug and endogenous biomarkers.

methodsIn vitro transporter-mediated substrate uptake and inhibition by ritlecitinib and its major metabolite were evaluated. Subsequently, a clinical drug interaction study was conducted in 12 healthy adult participants to assess the effect of ritlecitinib on pharmacokinetics of rosuvastatin, a substrate of breast cancer resistance protein (BCRP), organic anion transporting polypeptide 1B1 (OATP1B1), and organic anion transporter 3 (OAT3). Plasma concentrations of coproporphyrin I (CP-I) and pyridoxic acid (PDA) were assessed as endogenous biomarkers for OATP1B1 and OAT1/3 function, respectively.

resultsIn vitro studies suggested that ritlecitinib can potentially inhibit BCRP, OATP1B1 and OAT1/3 based on regulatory cutoffs. In the subsequent clinical study, coadministration of ritlecitinib decreased rosuvastatin plasma exposure area under the curve from time 0 to infinity (AUC

conclusionRitlecitinib does not inhibit BCRP, OATP1B1, and OAT3 and is unlikely to cause a clinically relevant interaction through these transporters. Furthermore, our findings add to the body of evidence supporting the utility of CP-I and PDA as endogenous biomarkers for assessment of OATP1B1 and OAT1/3 transporter activity.

Indexed as

Neoplasm ProteinsOrganic Anion TransportersAdultATP Binding Cassette Transporter, Subfamily G, Member 2BiomarkersDrug InteractionsHumansMembrane Transport ProteinsRosuvastatin CalciumATP Binding Cassette Transporter, Subfamily G, Member 2BiomarkersMembrane Transport ProteinsNeoplasm ProteinsOrganic Anion TransportersRosuvastatin Calciumdrug-drug interactionendogenous biomarkerritlecitinibrosuvastatin

Identifiers

PMID37561322
PMCPMC10733197
OpenAlexW4385716338

What OpenQuestion holds

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LicenceCC BY
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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.