Evidence map›Paper›PMID 40503733›Full record

ArticleBioanalysis2025

Quantitation of TAK-981 in human plasma via LC-MS/MS and its application in clinical trials.

Feng Yin, Ran Ye, Anson Pierce, John Gibbs, Mike Baratta

Abstract read
In one paragraph

Article in Bioanalysis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Feng YinTakeda Development Center Americas, Inc, Cambridge, MA, USA.ORCID 0000-0003-1655-3542
Ran YeTakeda Development Center Americas, Inc, Cambridge, MA, USA.
Anson PierceTakeda Development Center Americas, Inc, Cambridge, MA, USA.
John GibbsTakeda Development Center Americas, Inc, Cambridge, MA, USA.
Mike BarattaTakeda Development Center Americas, Inc, Cambridge, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTAK-981 is a highly effective and selective inhibitor of the small ubiquitin-like modifier (SUMO) activating enzyme, and it promotes the expression of type I interferons (IFN-Is). Developing a sensitive bioanalytical assay for quantitating TAK-981 is essential in the clinical investigations for oncology drug development. MATERIALS &

methodsTAK-981 and its stable isotope labeled compound (TAK-981

resultsThis assay was successfully validated from 0.1 ng/mL to 100 ng/mL with good accuracy and precision and has been applied to support clinical studies.

conclusionA sensitive and robust LC-MS/MS assay was validated for TAK-981 in human plasma for the first time.

Indexed as

Clinical Trials as TopicTandem Mass SpectrometryChromatography, LiquidHumansIsoquinolinesLiquid Chromatography-Mass SpectrometryPyrimidinesThiophenesIsoquinolinesPyrimidinesTAK-981ThiophenesclinicalLC-MS/MSoncologysmall moleculeSUMO activating enzyme inhibitorTAK-981validation

Identifiers

PMID40503733
PMCPMC12367096

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.