Evidence map›Paper›PMID 38232863›Full record

ArticleThe journal of pain2024

Discovery and Preclinical Evaluation of a Novel Inhibitor of FABP5, ART26.12, Effective in Oxaliplatin-Induced Peripheral Neuropathy.

George Warren, Myles Osborn, Christopher Tsantoulas, Ana David-Pereira, Daniel Cohn, Paul Duffy, Linette Ruston, Clare Johnson, Heather Bradshaw, Martin Kaczocha and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The journal of pain, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.1field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Evaluating FABP5 as a Therapeutic Target for Pain Management.European journal of pain (London, England) · 2026
    Review
  4. Article
  5. Combined intervention ofFrontiers in immunology · 2026
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. 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

13 authors at 1 institution in 1 country.

George WarrenArtelo Biosciences Limited, UK.
Myles OsbornArtelo Biosciences Limited, UK.
Christopher TsantoulasTranspharmation Ltd., London, UK.
Ana David-PereiraTranspharmation Ltd., London, UK.
Daniel CohnTranspharmation Ltd., London, UK.
Paul DuffyApconix Ltd., UK.
Linette RustonSeda Pharma Development Services Ltd., UK.
Clare JohnsonDepartment of Psychological and Brain Sciences, Bloomington, Indiana.
Heather BradshawDepartment of Psychological and Brain Sciences, Bloomington, Indiana.
Martin KaczochaDepartment of Anesthesiology, Stony Brook University, New York; Institute of Chemical Biology and Drug Discovery, Stony Brook University, New York.
Iwao OjimaDepartment of Chemistry, Stony Brook University, New York; Institute of Chemical Biology and Drug Discovery, Stony Brook University, New York.
Andrew YatesArtelo Biosciences Limited, UK.
Saoirse E O'SullivanArtelo Biosciences Limited, UK.
Mundipharma (United Kingdom) · GB

Funding

Anandamide Transport InhibitorsR01DA035923 · NIDA · STATE UNIVERSITY NEW YORK STONY BROOK · PI KACZOCHA, MARTIN · 2013 to 2017
$3.8M
FABPs: Novel Roles in Pain and InflammationR01DA035949 · NIDA · STATE UNIVERSITY NEW YORK STONY BROOK · PI KACZOCHA, MARTIN · 2014 to 2022
$3.0M
NIDA NIH HHS R01 DA035923NIDA NIH HHS R01 DA035949
6 · The paper itself

Abstract

Oxaliplatin-induced peripheral neuropathy (OIPN) is a dose-limiting toxicity characterised by mechanical allodynia and thermal hyperalgesia, without any licensed medications. ART26.12 is a fatty acid-binding protein (FABP) 5 inhibitor with antinociceptive properties, characterised here for the prevention and treatment of OIPN. ART26.12 binds selectively to FABP5 compared to FABP3, FABP4, and FABP7, with minimal off-target liabilities, high oral bioavailability, and a NOAEL of 1,000 mg/kg/day in rats and dogs. In an established preclinical OIPN model, acute oral dosing (25-100 mg/kg) showed a cannabinoid receptor type 1 (CB

Indexed as

Antineoplastic AgentsFatty Acid-Binding ProteinsHyperalgesiaOxaliplatinPeripheral Nervous System DiseasesAnalgesicsAnimalsDisease Models, AnimalDogsDose-Response Relationship, DrugDrug Evaluation, PreclinicalHumansMaleOrganoplatinum CompoundsRatsRats, Sprague-DawleyAnalgesicsAntineoplastic AgentsFatty Acid-Binding ProteinsOrganoplatinum CompoundsOxaliplatinCannabinoidChemotherapy-induced peripheral neuropathyFatty acid bind proteinLipidPain

Identifiers

PMID38232863
PMCPMC12993615
OpenAlexW4390988616

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.