Evidence map›Paper›PMID 38099236›Full record

ArticleItch (Philadelphia, Pa.)

Kappa opioid agonists in the treatment of itch: just scratching the surface?

Tyler C Beck, Elena M Wilson, Erik Wilkes, Lara Wine Lee, Russell Norris, Manuel Valdebran

Open access · hybridAbstract read
In one paragraph

Article in Itch (Philadelphia, Pa.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Xylazine and fentanyl co-administration delays wound healing in mice.bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

6 authors at 1 institution in 1 country.

Tyler C BeckDepartment of Dermatology and Dermatological Surgery, Medical University of South Carolina, Charleston, SC.
Elena M WilsonDepartment of Dermatology and Dermatological Surgery, Medical University of South Carolina, Charleston, SC.
Erik WilkesDepartment of Neuroscience, Medical University of South Carolina, Charleston, SC.
Lara Wine LeeDepartment of Dermatology and Dermatological Surgery, Medical University of South Carolina, Charleston, SC.
Russell NorrisDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC.
Manuel ValdebranDepartment of Dermatology and Dermatological Surgery, Medical University of South Carolina, Charleston, SC.
Medical University of South Carolina · US

Funding

Targeting Mek/Erk Signaling in the Treatment of Mitral Valve ProlapseF31HL158243 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BECK, TYLER · 2021 to 2023
$140k
NHLBI NIH HHS F31 HL158243
6 · The paper itself

Abstract

Chronic pruritus is a debilitating condition affecting 23-44 million Americans. Recently, kappa opioid agonists (KOAs) have emerged as a novel class of potent antipruritic agents. In 2021, the Food and Drug Administration approved difelikefalin (Korsuva) for the treatment of moderate-to-severe pruritus associated with chronic kidney disease in adults undergoing hemodialysis. Difelikefalin is a potent, peripherally restricted KOA that is intravenously available. Although promising, difelikefalin is currently available as an intravenous composition only, limiting the scope of use. Oral formulations of difelikefalin did not meet the primary endpoint criteria in recent phase 2 clinical trials; however, additional clinical studies are ongoing. The future for KOAs in the treatment of pruritus is encouraging. Orally active pathway-biased KOAs, such as triazole 1.1, may serve as viable alternatives with broader applications. Extended-release compositions, such as the TP-2021 ProNeura subdermal implant, may circumvent the pharmacokinetic issues associated with peptide-based KOAs. Lastly, dual-acting kappa opioid receptor agonist/mu opioid receptor antagonists are orally bioavailable and may be useful in the treatment of various forms of chronic itch. In this review, we summarize the results of KOAs in clinical and preclinical trials and discuss future directions of drug development.

Indexed as

AgonistDifelikefalinItchKappaOpioidPruritusTP-2021Triazole 1.1

Identifiers

PMID38099236
PMCPMC10720604
OpenAlexW4389400987

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.