Demyelinating disease

disease
On this page

Also known as demyelinating disorder

Summary

Demyelinating disease (MONDO:0002562) is a disease (an umbrella term covering 8 Mondo subtypes) and 27 clinical trials. Top therapeutic interventions include clemastine, ocrelizumab, and methotrexate. A subtype of neurodegenerative disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Umbrella term: 8 Mondo subtypes
  • Clinical trials: 27

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namedemyelinating disease
Mondo IDMONDO:0002562
MeSHD003711
DOIDDOID:3213
NCITC34527
UMLSC0011303
MedGen4189
Is cancer (heuristic)no

Also known as: demyelinating disorder

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 diseasedemyelinating disease

Related subtypes (21): synucleinopathy, eyelid degenerative disorder, senile degeneration of brain, olivopontocerebellar atrophy, neuroaxonal dystrophy, 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 (8): demyelinating polyneuropathy, central pontine myelinolysis, polyradiculoneuropathy, Schilder disease, Balo concentric sclerosis, acute disseminated encephalomyelitis, demyelinating disease of central nervous system, boylan dew greco syndrome

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): Amiloride.

Clinical trials & evidence

Clinical trials

Clinical trials: 27.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified16
PHASE14
PHASE1/PHASE23
PHASE41
PHASE31
PHASE21
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00037115PHASE4WITHDRAWNInduction Therapy With a Single High Dose Bolus of Intravenous Methotrexate With Leucovorin Rescue, Prior to Initiation of AVONEX® Treatment, in Patients Presenting With a First Acute Demyelinating Event.
NCT05834855PHASE3RECRUITINGNon-inferiority Study of Rituximab Compared to Ocrelizumab in Relapsing MS
NCT06065670PHASE1/PHASE2NOT_YET_RECRUITINGAssessing Changes in Multi-parametric MRI in Patients With Acute Demyelinating Lesions Taking Clemastine Fumarate as a Myelin Repair Therapy
NCT00001287PHASE2COMPLETEDIntravenous Immunoglobulin (IVIg) for the Treatment of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
NCT01056471PHASE1/PHASE2COMPLETEDAutologous Mesenchymal Stem Cells From Adipose Tissue in Patients With Secondary Progressive Multiple Sclerosis
NCT04539002PHASE1/PHASE2COMPLETEDAerobic Exercise for Remyelination in Multiple Sclerosis
NCT06999434PHASE1RECRUITINGExploring the Utility of [18F]3F4AP for Demyelination Imaging
NCT00283023PHASE1COMPLETEDOligodendrocyte Progenitor Cell Culture From Human Brain
NCT04710550PHASE1UNKNOWNExploring the Utility of [18F]3F4AP for Demyelination Imaging in Controls, Neurodegeneration and Traumatic Brian Injury
NCT06677710PHASE1SUSPENDEDIDP-023 g-NK Cells Plus Ocrelizumab in Patients With Progressive Multiple Sclerosis
NCT06985303EARLY_PHASE1WITHDRAWNCell-Based Therapy for White Matter Repair in Periventricular Leukomalacia
NCT06494228Not specifiedRECRUITINGComparison of Diagnostic Performances of 3D FLAIR, DIR and PSIR Sequences in Optic Neuritis
NCT06534177Not specifiedNOT_YET_RECRUITINGDigital Diagnostics and Intervention Services for Parkinson’s Disease
NCT06541626Not specifiedRECRUITINGSun Yat-Sen Cohort of CNS Idiopathic Inflammatory Demyelinating Diseases
NCT06573723Not specifiedRECRUITINGInstitutional Registry of Rare Diseases
NCT00001780Not specifiedCOMPLETEDMagnetic Stimulation of the Human Nervous System
NCT01963650Not specifiedTERMINATEDNatural History Study of Children With Metachromatic Leukodystrophy
NCT03010826Not specifiedCOMPLETEDPharmacological Recruitment of Endogenous Neural Precursors to Promote Pediatric White Matter Repair: Establishing Correlations Between Visual Outcomes, Saccadic Function and MEG Oscillations in Children With Demyelinating Disorders in Comparison to Healthy Control Children
NCT03268239Not specifiedCOMPLETEDContrast-enhanced 3D T1-weighted Gradient-echo Versus Spin-echo 3 Tesla MR Sequences in the Detection of Active Multiple Sclerosis Lesions
NCT03562975Not specifiedCOMPLETEDUpper Extremity Function in Multiple Sclerosis Patients With Advanced Disability Treated With Ocrevus
NCT04762342Not specifiedUNKNOWNPower Training in Older Multiple Sclerosis Patients
NCT04837651Not specifiedCOMPLETEDHumoral and T-Cell Responses to COVID-19 Vaccination in Multiple Sclerosis Patients Treated With Ocrelizumab Treated With Ocrelizumab or Natalizumab
NCT04997343Not specifiedUNKNOWNNeurophysiological Assessment in Patients With Multiple Sclerosis
NCT05199363Not specifiedUNKNOWNPediatric Patient Experience on a Diagnostic Path
NCT05605951Not specifiedUNKNOWNAcute Optic Neuritis Network: an International Study That Invesitages Subjects With a First-ever Episode of Acute Inflammation of the Optic Nerve
NCT05792176Not specifiedCOMPLETEDUkulele Playing to Improve Cognition in People with Multiple Sclerosis: a Feasibility Study
NCT06019611Not specifiedCOMPLETEDEpidural Stimulation in Multiple Sclerosis

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CLEMASTINE43
OCRELIZUMAB42
METHOTREXATE41
METHYLPREDNISOLONE41
INTERFERON BETA31
CHEMBL42601