Prurigo

disease
On this page

Also known as Itchy skin eruptionPruritic rash

Summary

Prurigo (MONDO:0021739) is a disease with 2 GWAS associations across 6 studies and 6 clinical trials. Top therapeutic interventions include abrocitinib, nalbuphine, and ruxolitinib. A subtype of exanthem — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 2
  • Clinical trials: 6

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameprurigo
Mondo IDMONDO:0021739
MeSHD011536
ICD-11268810206
SNOMED CT64144002
UMLSC0033771
MedGen10986
Is cancer (heuristic)no

Also known as: Itchy skin eruption · prurigo · Pruritic rash · pruritic rash

Data availability: 2 GWAS associations (6 studies).

Disease family

This is a subtype of exanthem. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › integumentary system disorder › skin disorderexanthemprurigo

Related subtypes (12): exanthema subitum, variola major infectious disease, pityriasis versicolor, bacterial exanthem, pityriasis rosea, viral exanthem, pityriasis lichenoides, pityriasis simplex, pityriasis folliculorum, pityriasis amiantacea, pityriasis alba, pityriasis steatoides

Genetics & variants

GWAS landscape

2 GWAS associations across 6 studies. Top hits map to 0 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs1848897464e-31HLA-DRB9 - HLA-DRB5T0.6
chr6:325493627e-27G0.41

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90478795Verma A20247,448432,972Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90476184Verma A20243,810114,442Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480455Verma A20243,810114,442Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90478794Verma A20241,19357,395Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90436602Zhou W2018779402,672Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
GCST90727032Kim HI202670143,325Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic2

MAF distribution

BucketVariants
common (>=0.05)1
low_freq (0.01-0.05)1
rare (<0.01)0
unknown0

Functional consequences

ConsequenceCount
intron_variant1
unknown1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs184889746632486608T>C0.012intron_variantHLA-DRB9 - HLA-DRB54e-31Tier 4: intronic/intergenic
chr6:325493620.0887e-27Tier 4: intronic/intergenic

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated for this disease

2 approved, 1 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
DupilumabApproved (phase 4)
NemolizumabApproved (phase 4)
RuxolitinibPhase 3 (in late-stage trials)

Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Benralizumab.

Clinical trials & evidence

Clinical trials

Clinical trials: 6.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE2/PHASE32
PHASE22
PHASE31
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02174419PHASE2/PHASE3COMPLETEDStudy of Nalbuphine HCl ER Tablets in Patients With Prurigo Nodularis
NCT02174432PHASE2/PHASE3COMPLETEDOpen Label Extension Study of Nalbuphine HCl ER in Patients With Prurigo Nodularis
NCT05755438PHASE3COMPLETEDA Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Participants With Prurigo Nodularis (PN)
NCT05038982PHASE2COMPLETEDEfficacy of Abrocitinib for Reducing Pruritus in Adults With Prurigo Nodularis and Chronic Pruritus of Unknown Origin
NCT05528913PHASE2WITHDRAWNBenralizumab in Chronic Prurigo - Investigating Clinical Efficacy (BICPIC)
NCT03340155Not specifiedUNKNOWNMechanisms of Action of Photo(Chemo)Therapy in Skin Diseases

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ABROCITINIB41
NALBUPHINE41
RUXOLITINIB41
CHEMBL463716301