Arteriosclerosis obliterans

disease
On this page

Also known as arteriosclerosis obliterans (disorder) [ambiguous]

Summary

Arteriosclerosis obliterans (MONDO:0006659) is a disease and 10 clinical trials. Top therapeutic interventions include cilostazol, alprostadil, and probucol. A subtype of coronary atherosclerosis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 10

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namearteriosclerosis obliterans
Mondo IDMONDO:0006659
EFOEFO:1000820
MeSHD001162
DOIDDOID:5160
SNOMED CT361133006
UMLSC0003851
MedGen13915
MedDRA10065418
Is cancer (heuristic)no

Also known as: arteriosclerosis obliterans (disorder) [ambiguous]

Disease family

This is a subtype of coronary atherosclerosis. 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 › cardiovascular disordervascular disorderarterial disordercoronary artery disordercoronary atherosclerosisarteriosclerosis obliterans

Related subtypes (1): arteriolosclerosis

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

Drugs indicated for this disease

No approved or late-stage (phase ≥3) drug is indicated for this disease; the following are in earlier-phase trials only.

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

Clinical trials & evidence

Clinical trials

Clinical trials: 10.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified6
PHASE42
PHASE1/PHASE21
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00823849PHASE4COMPLETEDStudy of Cilostazol and Probucol to Assess Their Effects on Atherosclerosis Related Biomarker
NCT00912756PHASE4UNKNOWNSufficient Treatment of Peripheral Intervention by Cilostazol
NCT02864654PHASE1/PHASE2UNKNOWNEffectiveness and Safety of Adipose-Derived Regenerative Cells for the Treatment of Critical Lower Limb Ischemia
NCT02877173PHASE2UNKNOWNA Safety/Efficacy Study of Alprostadil Liposomes for Injection to Treat Lower Extremity Arteriosclerosis Obliterans
NCT06485622Not specifiedRECRUITINGOutcome and Improvement of Different Treatment in Arteriosclerosis Obliterans
NCT07023965Not specifiedENROLLING_BY_INVITATIONFollow-up Study Using Gene Therapy for Critical Limb Ischemia (NL003-CLI-III-L)
NCT00145262Not specifiedUNKNOWNTACT-NAGOYA: Therapeutic Angiogenesis Using Cell Transplantation
NCT00712946Not specifiedCOMPLETEDPreoperative Heart Rate Variability and Baroreflex Sensitivity in ASO Patients During Various Sleep Stages
NCT01518205Not specifiedCOMPLETEDHELP-Apheresis in Diabetic Ischemic Foot Treatment (H.A.D.I.F)
NCT02431234Not specifiedUNKNOWNArterial Calcification in the Diabetes

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CILOSTAZOL42
ALPROSTADIL41
PROBUCOL41
CHEMBL44323201