Fournier gangrene

disease
On this page

Also known as Fournier diseaseFournier's diseaseFournier's gangreneFourniers diseaseFourniers gangrenegangrene, Fourniergangrene, Fournier's

Summary

Fournier gangrene (MONDO:0043352) is a disease and 13 clinical trials. Top therapeutic interventions include sodium chloride, daptomycin, and reltecimod. A subtype of male reproductive system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 13

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namefournier gangrene
Mondo IDMONDO:0043352
MeSHD018934
ICD-10-CMN49.3
SNOMED CT398318005
UMLSC0238419
MedGen65967
Is cancer (heuristic)no

Also known as: Fournier disease · fournier gangrene · Fournier’s disease · Fournier’s gangrene · fournier’s gangrene · Fourniers disease · Fourniers gangrene · gangrene, Fournier · gangrene, Fournier’s

Disease family

This is a subtype of male reproductive system disorder. 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 › reproductive system disordermale reproductive system disorderfournier gangrene

Related subtypes (25): benign male reproductive system neoplasm, hematocele of tunica vaginalis testis, male genital organ stricture, male genital organ vascular disease, penile disorder, testicular disorder, prostate disorder, epididymitis, hydrocele, male infertility, male genital tuberculosis, spermatocele, dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome, cryptorchidism, diphallia, postorgasmic illness syndrome, penoscrotal transposition, congenital bilateral absence of vas deferens, posterior hypospadias, isolated micropenis, male reproductive system neoplasm, congenital agenesis of the scrotum, scrotal disorder, congenital megaprepuce, epididymis disease

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: 13.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified11
PHASE31
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02469857PHASE3COMPLETEDPhase III Efficacy and Safety Study of AB103 in the Treatment of Patients With Necrotizing Soft Tissue Infections
NCT02111161PHASE2COMPLETEDImmunoglobulin for Necrotizing Soft Tissue Infections: a Randomised Controlled Trial
NCT07107555Not specifiedENROLLING_BY_INVITATIONNecrotizing Soft Tissue Infections
NCT07359651Not specifiedRECRUITINGFATAL-NSTI Study (Factors Associated With In-hospital mortALity in NSTI).
NCT00261807Not specifiedCOMPLETEDDaptomycin for the Treatment of Severe Necrotizing Soft-Tissue Infections
NCT02180906Not specifiedCOMPLETEDBiomarkers in Patients With Flesh-eating Bacterial Infections
NCT02501382Not specifiedCOMPLETEDModulation of Biomarkers in Patients With Flesh-eating Bacterial Infections After With Hyperbaric Oxygen Treatment
NCT03147352Not specifiedCOMPLETEDPrognosis and Treatment of Necrotizing Soft Tissue Infections: A Prospective Cohort Study
NCT03443544Not specifiedCOMPLETEDFournier’s Gangrene and the Origin of the Infection as a Prognostic of Morbidity and Mortality, an Analysis of 121 Patients
NCT04694053Not specifiedCOMPLETEDFournier’s Gangrene in Patient With Uncontrolled Type 2 Diabetes
NCT04983056Not specifiedCOMPLETEDManagement of Fournier Gangrene at Ibn Rochd University Hospital Center
NCT05116956Not specifiedUNKNOWNSKin and Soft Tissue Necrotizing INfections in the Intensive Care Unit: a Prospective Multi-national Cohort Study
NCT05529628Not specifiedCOMPLETEDThe Immunological Differences Between Fournier Gangrene and Perianal Abscess

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
SODIUM CHLORIDE42
DAPTOMYCIN41
RELTECIMOD31
CHEMBL164972201
CHEMBL428678401
CHEMBL474444401