Evidence map›Paper›PMID 41355395›Full record

ArticleInternational journal of clinical pharmacology and therapeutics2026

Population pharmacokinetics of tofacitinib in patients with active ankylosing spondylitis.

Shinichi Tsuchiwata, Akiyuki Suzuki, Qiang Wang, Keith Kanik, Lara Fallon, Sujatha Menon

Abstract read
In one paragraph

Article in International journal of clinical pharmacology and therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Shinichi Tsuchiwata
Akiyuki Suzuki
Qiang Wang
Keith Kanik
Lara Fallon
Sujatha Menon

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterize tofacitinib pharmacokinetics (PK) in patients with active ankylosing spondylitis (AS) and estimate the effects of covariates on variability of PK parameters. MATERIALS AND

methodsPooled data from two studies in patients with AS who received tofacitinib were analyzed using nonlinear mixed-effects modeling. Tofacitinib PK was described by a one-compartment model parameterized in terms of apparent oral clearance (CL/F), apparent volume of distribution (V/F), and a first-order absorption rate constant (k

resultsAnalysis included 279 patients. The point estimates for CL/F, V/F, and k

conclusionTofacitinib does not require dose adjustment/restriction for age, body weight, sex, or race based on the differences (< 20%) in exposure relative to a reference patient with AS. The tofacitinib CL/F and BCCL relationship was consistent with known contribution of renal excretion to total tofacitinib clearance.

Indexed as

Models, BiologicalPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolesSpondylitis, AnkylosingAdultAgedArea Under CurveFemaleHumansMaleMiddle AgedNonlinear DynamicsYoung AdultPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolestofacitinib

Identifiers

PMID41355395
PMCPMC12825014

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LicenceCC BY
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Registered trials

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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.