Synucleinopathy

disease
On this page

Summary

Synucleinopathy (MONDO:0000510) is a disease and 15 clinical trials. Top therapeutic interventions include donanemab, idebenone, and rasagiline. A subtype of neurodegenerative disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 15

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namesynucleinopathy
Mondo IDMONDO:0000510
MeSHD000080874
DOIDDOID:0050890
UMLSC5191670
MedGen1682194
GARD0022781
Is cancer (heuristic)no

Disease family

This is a subtype of neurodegenerative disease. 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 › nervous system disordercentral nervous system disorderneurodegenerative diseasesynucleinopathy

Related subtypes (21): eyelid degenerative disorder, senile degeneration of brain, olivopontocerebellar atrophy, neuroaxonal dystrophy, demyelinating disease, choroidal sclerosis, tauopathy, secondary Parkinson disease, infantile bilateral striatal necrosis, Marchiafava-Bignami disease, superficial siderosis, primary progressive apraxia of speech, human prion disease, primary progressive freezing gait, primary progressive aphasia, motor neuron disorder, brachial amyotrophic diplegia, cerebellar degeneration, inherited neurodegenerative disorder, cerebral degeneration, hypertrophic olivary degeneration

Subtypes (2): Lewy body dementia, multiple system atrophy

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: 15.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified10
PHASE23
PHASE2/PHASE31
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05611372PHASE2/PHASE3WITHDRAWNEfficacy and Safety of Rasagiline in Prodromal Parkinson’s Disease
NCT04534023PHASE2ACTIVE_NOT_RECRUITINGA Clinical Study of the Efficacy of Idebenone in the Treatment of iRBD Into Synucleinopathies
NCT06460038PHASE2RECRUITINGTenapanor in Synucleinopathy-Related Constipation
NCT07589595PHASE2NOT_YET_RECRUITINGA Study of Donanemab (LY3002813) in Participants With Early Cognitive Decline (TRAILBLAZER-ALZ 7)
NCT06827821EARLY_PHASE1NOT_YET_RECRUITINGApplication of 18F-CP6A PET Imaging in Synucleinopathies
NCT06193252Not specifiedRECRUITINGSlow-SPEED-NL: Slowing Parkinson’s Early Through Exercise Dosage-Netherlands
NCT06534177Not specifiedNOT_YET_RECRUITINGDigital Diagnostics and Intervention Services for Parkinson’s Disease
NCT06596746Not specifiedRECRUITINGNeurodegenerative Diseases Progression Markers (MARKERS-NDD)
NCT06993142Not specifiedNOT_YET_RECRUITINGSlow-SPEED: Slowing Parkinson’s Early Through Exercise Dosage
NCT07187843Not specifiedRECRUITINGStudy of Axial and Cognitive Symptoms and Biomarkers of Neurodegeneration in Brain-first and Body-first PD
NCT07324330Not specifiedRECRUITINGSlowing Cognitive Decline in Alpha-synucleinopathies by Enhancing Physical Activity
NCT07480187Not specifiedACTIVE_NOT_RECRUITINGToward Molecular Profiling of Parkinson’s Disease in Easily Accessible Biological Matrices
NCT07533799Not specifiedRECRUITINGThe Swedish BioFINDER Sleep Study
NCT05452655Not specifiedUNKNOWNIntensive Multidisciplinary Rehabilitation and Biomarkers in Parkinson’s Disease
NCT05486806Not specifiedUNKNOWNLongitudinal Tracking of Patients Diagnosed With Neurodegenerative Movement Disorders

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
DONANEMAB41
IDEBENONE41
RASAGILINE41
TENAPANOR41