Prurigo
diseaseOn 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
| Field | Value |
|---|---|
| Canonical name | prurigo |
| Mondo ID | MONDO:0021739 |
| MeSH | D011536 |
| ICD-11 | 268810206 |
| SNOMED CT | 64144002 |
| UMLS | C0033771 |
| MedGen | 10986 |
| 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 disorder › exanthem › prurigo
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
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs184889746 | 4e-31 | HLA-DRB9 - HLA-DRB5 | T | 0.6 |
| chr6:32549362 | 7e-27 | G | 0.41 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90478795 | Verma A | 2024 | 7,448 | 432,972 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90476184 | Verma A | 2024 | 3,810 | 114,442 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90480455 | Verma A | 2024 | 3,810 | 114,442 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90478794 | Verma A | 2024 | 1,193 | 57,395 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90436602 | Zhou W | 2018 | 779 | 402,672 | Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. |
| GCST90727032 | Kim HI | 2026 | 701 | 43,325 | Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 0 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 2 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 1 |
| low_freq (0.01-0.05) | 1 |
| rare (<0.01) | 0 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 1 |
| unknown | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs184889746 | 6 | 32486608 | T>C | 0.012 | intron_variant | HLA-DRB9 - HLA-DRB5 | 4e-31 | Tier 4: intronic/intergenic |
| chr6:32549362 | 0.088 | 7e-27 | Tier 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.
| Drug | Development status |
|---|---|
| Dupilumab | Approved (phase 4) |
| Nemolizumab | Approved (phase 4) |
| Ruxolitinib | Phase 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)
| Phase | Trials |
|---|---|
| PHASE2/PHASE3 | 2 |
| PHASE2 | 2 |
| PHASE3 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02174419 | PHASE2/PHASE3 | COMPLETED | Study of Nalbuphine HCl ER Tablets in Patients With Prurigo Nodularis |
| NCT02174432 | PHASE2/PHASE3 | COMPLETED | Open Label Extension Study of Nalbuphine HCl ER in Patients With Prurigo Nodularis |
| NCT05755438 | PHASE3 | COMPLETED | A Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Participants With Prurigo Nodularis (PN) |
| NCT05038982 | PHASE2 | COMPLETED | Efficacy of Abrocitinib for Reducing Pruritus in Adults With Prurigo Nodularis and Chronic Pruritus of Unknown Origin |
| NCT05528913 | PHASE2 | WITHDRAWN | Benralizumab in Chronic Prurigo - Investigating Clinical Efficacy (BICPIC) |
| NCT03340155 | Not specified | UNKNOWN | Mechanisms of Action of Photo(Chemo)Therapy in Skin Diseases |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| ABROCITINIB | 4 | 1 |
| NALBUPHINE | 4 | 1 |
| RUXOLITINIB | 4 | 1 |
| CHEMBL4637163 | 0 | 1 |
Related Atlas pages
- Drugs: Abrocitinib, Nalbuphine, Ruxolitinib