Evidence map›Paper›PMID 41401055›Full record

Trial reportJournal of the European Academy of Dermatology and Venereology : JEADV2026

Rapid improvement of itch with nemolizumab in atopic dermatitis and prurigo nodularis phase 3 studies.

Sonja Ständer, Sarina B Elmariah, Shawn G Kwatra, Gil Yosipovitch, Andrew E Pink, Soo Yeon Cheong, Xiaoxiao Chen, Zarif K Jabbar-Lopez, Liliana Ulianov, Christophe Piketty and 1 more

Abstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of the European Academy of Dermatology and Venereology : JEADV, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Rapid improvement of itch with nemolizumab in atopic dermatitis and prurigo nodularis phase 3 studies.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Trial
  2. Article
  3. Immunopathogenesis of itch: an integrative framework for chronic pruritus.JID innovations : skin science from molecules to population health · 2026
    Review
  4. Review
  5. 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

11 authors.

Sonja StänderSection Pruritus Medicine, Department of Dermatology and Center for Chronic Pruritus, University Hospital Münster, Münster, Germany.ORCID https://orcid.org/0000-0003-3612-7786
Sarina B ElmariahUniversity of California San Francisco Center for Itch and Neurosensory Disorders, San Francisco, California, USA.
Shawn G KwatraDepartment of Dermatology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Gil YosipovitchDr Philip Frost Department of Dermatology and Cutaneous Surgery, Miller School of Medicine, Miami Itch Center, University of Miami, Miami, Florida, USA.
Andrew E PinkSt John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust and King's College London, London, UK.
Soo Yeon CheongGalderma Laboratories, LP, Dallas, Texas, USA.
Xiaoxiao ChenGalderma Laboratories, LP, Dallas, Texas, USA.
Zarif K Jabbar-LopezGalderma Research and Development, Zug, Switzerland.
Liliana UlianovGalderma Research and Development, Zug, Switzerland.
Christophe PikettyGalderma Laboratories, LP, Dallas, Texas, USA.ORCID https://orcid.org/0000-0002-9969-2478
Jonathan I SilverbergDepartment of Dermatology, The George Washington School of Medicine and Health Sciences, Washington, DC, USA.ORCID https://orcid.org/0000-0003-3686-7805

Funding

Galderma
6 · The paper itself

Abstract

BACKGROUND/

objectivesItch is the most burdensome symptom in atopic dermatitis (AD) and prurigo nodularis (PN) and is associated with significant psychological distress, sleep deprivation and impaired quality of life. Achieving rapid control of itch is expected to minimize symptomatology and disease burden. Nemolizumab, which targets the interleukin 31 (IL-31) pathway, rapidly relieved itch in Phase 2 trials; thus, a post hoc analysis of four pivotal randomized controlled clinical trials of nemolizumab in AD and PN was performed to further evaluate the improvement of itch over the first 14 days of therapy.

methodsData from ARCADIA 1 and 2 in AD (N = 1728) and OLYMPIA 1 and 2 in PN (N = 560) were analysed. Patients reported itch intensity and sleep disturbance daily. Differences in the proportion of itch and sleep responders (patients with ≥4-point improvement from baseline in peak pruritus numerical rating scale [PP-NRS] or sleep disturbance [SD-NRS] score) between nemolizumab and placebo groups were calculated.

resultsNemolizumab rapidly reduced itch in AD (ARCADIA 1 and 2), with a difference versus placebo in PP-NRS responders apparent by Day 2 (pooled data: 10.7% vs. 2.9%; 95% CI: 5.6-10.1; p < 0.0001) that steadily increased through Day 14. Nemolizumab also reduced itch rapidly in PN (OLYMPIA 1 and 2); a difference versus placebo occurred by Day 2 (pooled data: 17.2% vs. 3.7%; 95% CI: 6.8-16.7; p < 0.0001). Early improvement (Day 2) was also observed in sleep in nemolizumab-treated patients. In pooled analyses in AD, 9.9% (nemolizumab) versus 4.6% (placebo; 95% CI: 2.8-7.7; p = 0.0001) were SD-NRS responders and in PN, 13.4% versus 4.3% (95% CI: 4.0-13.0; p = 0.0013). Itch and sleep response data in individual studies were consistent with the pooled data.

conclusionsThis analysis confirms previously reported data that nemolizumab relieves itch and sleep disturbance by Day 2 in patients with moderate-to-severe AD and PN, indicating that targeting the IL-31 pathway presents an important way to achieve rapid itch response.

Indexed as

Antibodies, Monoclonal, HumanizedDermatitis, AtopicPrurigoPruritusAdolescentAdultFemaleHumansMaleMiddle AgedYoung AdultAntibodies, Monoclonal, Humanizednemolizumabatopic dermatitiseczematous diseaseinterleukin 31itchnemolizumabonset of actionprurigo nodularispruritussleep disturbance

Identifiers

PMID41401055
PMCPMC13109751

What OpenQuestion holds

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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.