Melancholia

disease
On this page

Also known as depression with melancholic featuresmelancholic depression

Summary

Melancholia (MONDO:0002444) is a disease and 6 clinical trials. Top therapeutic interventions include fluvoxamine, lamotrigine, and nortriptyline. A subtype of depressive disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 6

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namemelancholia
Mondo IDMONDO:0002444
EFOEFO:1002014
DOIDDOID:2848
NCITC34812
UMLSC0025193
MedGen6288
Is cancer (heuristic)no

Also known as: depression with melancholic features · melancholic depression

Disease family

This is a subtype of depressive 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 developmental or physiological process › psychiatric disordermental disordermood disorderdepressive disordermelancholia

Related subtypes (6): seasonal affective disorder, major depressive disorder, postpartum depression, bipolar depression, neurotic depression, mixed anxiety and depressive disorder

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

1 approved. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
FluvoxamineApproved (phase 4)

Clinical trials & evidence

Clinical trials

Clinical trials: 6.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE42
PHASE22
Not specified2

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00000378PHASE4COMPLETEDAntidepressant Treatment of Melancholia in Late Life
NCT02989727PHASE4COMPLETEDMelancholic Symptoms in Bipolar Depression and Responsiveness to Lamotrigine
NCT01548937PHASE2COMPLETEDSerotonin Transporter Density in Late-life Depression With and Without Dementia
NCT04160377PHASE2UNKNOWNA Clinical Trial of Fluvoxamine for Melancholia
NCT00971815Not specifiedCOMPLETEDEffects of 3 Months of Selective Serotonin Reuptake Inhibitor (SSRI)-Treatment on Metabolism and Hypothalamic-pituitary-adrenal (HPA)-Axis in Young Men Born With Low Birth Weight
NCT03288675Not specifiedCOMPLETEDStepped Care AiTBS 2 Depression Study (Ghent)

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
FLUVOXAMINE43
LAMOTRIGINE41
NORTRIPTYLINE41
SERTRALINE41
CHEMBL178836101