Evidence map›Paper›PMID 36369799›Full record

ArticleClinical pharmacology in drug development2023

Pharmacokinetics of the Multi-kinase Inhibitor Pexidartinib: Mass Balance and Dose Proportionality.

Hamim Zahir, Jonathan Greenberg, Ching Hsu, Kengo Watanabe, Chie Makino, Ling He, Frank LaCreta

Open access · hybridAbstract read
In one paragraph

Article in Clinical pharmacology in drug development, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 3 institutions in 3 countries.

Hamim ZahirDaiichi Sankyo, Inc, Basking Ridge, New Jersey, USA.
Jonathan GreenbergDaiichi Sankyo, Inc, Basking Ridge, New Jersey, USA.
Ching HsuDaiichi Sankyo, Inc, Basking Ridge, New Jersey, USA.
Kengo WatanabeDaiichi Sankyo Co, Ltd., Tokyo, Japan.
Chie MakinoDaiichi Sankyo Co, Ltd., Tokyo, Japan.
Ling HeDaiichi Sankyo, Inc, Basking Ridge, New Jersey, USA.
Frank LaCretaDaiichi Sankyo, Inc, Basking Ridge, New Jersey, USA.
Daiichi Sankyo (United States) · USDaiichi Sankyo (Germany) · DEDaiichi-Sankyo (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pexidartinib is an oral small-molecule tyrosine kinase inhibitor that selectively targets colony-stimulating factor 1 receptor. Two phase 1 single-center trials were conducted in healthy subjects to determine the absorption, distribution, metabolism, and excretion of pexidartinib using radiolabeled drug and to assess the dose proportionality of pexidartinib following single oral doses. In the mass balance study, eight male subjects received a single oral dose of [

Indexed as

Antineoplastic AgentsGlucuronidesAminopyridinesHumansMaleProtein Kinase InhibitorsPyrrolesAminopyridinesAntineoplastic AgentsGlucuronidespexidartinibProtein Kinase InhibitorsPyrrolesdose proportionalitymass balancemulti-kinase inhibitorpexidartinibpharmacokineticsZAAD-1006a

Identifiers

PMID36369799
PMCPMC10099993
OpenAlexW4308834322

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.