Bladder urachal adenocarcinoma
diseaseOn this page
Also known as adenocarcinoma of the urachusurachal adenocarcinomaurachus adenocarcinoma
Summary
Bladder urachal adenocarcinoma (MONDO:0004331) is a disease and 2 clinical trials. Top therapeutic interventions include cabozantinib, enfortumab vedotin, and ipilimumab. A subtype of urachus cancer — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 2
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | bladder urachal adenocarcinoma |
| Mondo ID | MONDO:0004331 |
| MeSH | C536474 |
| DOID | DOID:7694 |
| NCIT | C39843 |
| UMLS | C2931201 |
| MedGen | 419014 |
| GARD | 0010186 |
| Anatomy (UBERON) | UBERON:0002068 |
| Is cancer (heuristic) | no |
Also known as: adenocarcinoma of the urachus · bladder urachal adenocarcinoma · urachal adenocarcinoma · urachus adenocarcinoma
Data availability: 1 cell line.
Disease family
Classification path: disease › human disease › disease by body system or component › urinary system disorder › urinary bladder disorder › urinary bladder neoplasm › urinary bladder cancer › urachus cancer › bladder urachal adenocarcinoma
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
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
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 2.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03866382 | PHASE2 | RECRUITING | Testing the Effectiveness of Two Immunotherapy Drugs (Nivolumab and Ipilimumab) With One Anti-cancer Targeted Drug (Cabozantinib) for Rare Genitourinary Tumors |
| NCT05756569 | PHASE2 | RECRUITING | Enfortumab Vedotin Plus Pembrolizumab for the Treatment of Locally Advanced or Metastatic Bladder Cancer of Variant Histology |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CABOZANTINIB | 4 | 3 |
| ENFORTUMAB VEDOTIN | 4 | 1 |
| IPILIMUMAB | 4 | 1 |
Related Atlas pages
- Drugs: Cabozantinib, Enfortumab Vedotin, Ipilimumab