Guillain-Barre syndrome

disease
On this page

Also known as acute autoimmune peripheral neuropathyacute immune-mediated polyneuropathyacute inflammatory demyelinating polyneuropathyacute inflammatory neuropathyGBSGuillain Barre syndromeGuillain Barré syndromeGuillain-Barre-Strohl syndromeGuillain-Barré syndromeGuillain-Barré-Strohl syndromeLandry's ascending paralysisLandry-Guillain-Barre-Strohl syndromepost-infectious polyneuritispost-infective polyneuritispostinfectious polyneuritis

Summary

Guillain-Barre syndrome (MONDO:0016218) is a disease (an umbrella term covering 11 Mondo subtypes) and 79 clinical trials. Top therapeutic interventions include efgartigimod alfa, crovalimab, and dalfampridine. A subtype of autoimmune disorder of peripheral nervous system — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: 1-9 / 100 000 (Europe) [Orphanet-validated]
  • Umbrella term: 11 Mondo subtypes
  • Clinical trials: 79

Clinical features

Epidemiology

Prevalence records

7 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Annual incidence1-9 / 100 0001.45WorldwideValidated
Point prevalence1-9 / 100 0003.5EuropeValidated
Annual incidence1-9 / 100 0001.72United StatesValidated
Annual incidence1-9 / 100 0002.42FranceValidated
Point prevalence1-5 / 10 00025DenmarkValidated
Point prevalence1-5 / 10 00012EgyptValidated
Annual incidence1-9 / 100 0001.4EuropeNot yet validated

Identifiers

Disease identifiers

FieldValue
Canonical nameGuillain-Barre syndrome
Mondo IDMONDO:0016218
EFOEFO:0007292
MeSHD020275
Orphanet2103
DOIDDOID:12842
ICD-10-CMG61.0
NCITC116345
SNOMED CT40956001
UMLSC0018378
MedGen5399
GARD0006554
MedDRA10018767
Is cancer (heuristic)no

Also known as: acute autoimmune peripheral neuropathy · acute immune-mediated polyneuropathy · acute inflammatory demyelinating polyneuropathy · acute inflammatory neuropathy · GBS · Guillain Barre syndrome · Guillain Barré syndrome · Guillain-Barre-Strohl syndrome · Guillain-Barré syndrome · Guillain-Barré-Strohl syndrome · Landry’s ascending paralysis · Landry-Guillain-Barre-Strohl syndrome · post-infectious polyneuritis · post-infective polyneuritis · postinfectious polyneuritis

Data availability: 6 cell lines.

Disease family

This is a subtype of autoimmune disorder of peripheral nervous system. 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 disorderautoimmune disorder of the nervous systemautoimmune disorder of peripheral nervous systemGuillain-Barre syndrome

Related subtypes (3): autoimmune neuropathy, myasthenia gravis, autoimmune optic neuritis

Subtypes (11): Guillain-Barre syndrome, familial, pharyngeal-cervical-brachial variant of Guillain-Barre syndrome, paraparetic variant of Guillain-Barre syndrome, acute pure sensory neuropathy, autoimmune autonomic ganglionopathy, acute sensory ataxic neuropathy, facial diplegia with paresthesias, acute inflammatory demyelinating polyradiculoneuropathy, acute motor and sensory axonal neuropathy, acute motor axonal neuropathy, polyneuropathy, inflammatory demyelinating, chronic

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 or in trials for this disease

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

DrugStatus
Human Immunoglobulin GApproved (phase 4)

6 drugs in clinical trials for this disease (phase 2–3, investigational): efficacy not established — a trial record, not an indication.

DrugHighest phase
ANX-005Phase 3
CrovalimabPhase 3
EculizumabPhase 3
DalfampridinePhase 2
Efgartigimod AlfaPhase 2
ImlifidasePhase 2

Clinical trials & evidence

Clinical trials

Clinical trials: 79.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified60
PHASE36
PHASE25
PHASE42
PHASE2/PHASE32
PHASE12
PHASE1/PHASE21
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06620198PHASE4ACTIVE_NOT_RECRUITINGUpper Limb Robot-Assisted Therapy in Patients with Guillain-Barré Syndrome
NCT06041451PHASE4UNKNOWNEarly and Late Prognosis in Patients With Guillain-Barre Syndrome
NCT06885762PHASE2/PHASE3NOT_YET_RECRUITINGEfgartigimod for the Treatment of Guillain-Barré Syndrome
NCT07020819PHASE3RECRUITINGAn Open Label Clinical Study to Evaluate Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (FORWARD Study)
NCT02221271PHASE3COMPLETEDPhase III Clinical Trial of NPB-01 in Patients With Guillain-Barré Syndrome
NCT02342184PHASE3COMPLETEDEfficacy and Safety Study of GB-0998 for Guillain-Barré Syndrome
NCT04701164PHASE3COMPLETEDEfficacy and Safety of ANX005 in Subjects With Guillain-Barré Syndrome
NCT04752566PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Eculizumab in Guillain-Barré Syndrome
NCT05104762PHASE2/PHASE3COMPLETEDIVIG Versus Plasmapheresis in the Treatment of Guillian Barrie Syndrome Patients
NCT05494619PHASE3WITHDRAWNA Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Participants With Guillain-Barré Syndrome (GBS)
NCT00056810PHASE2COMPLETEDAssessment of Chronic Guillain-Barre Syndrome Improvement With Use of 4-aminopyridine
NCT00167622PHASE2COMPLETEDEarly Mechanical Ventilation for Guillain Barré Syndrome
NCT02780570PHASE2COMPLETEDSmall Volume Plasma Exchange (SVPE) for Guillain-Barré Syndrome (GBS) Patients
NCT03943589PHASE2COMPLETEDA Study of Imlifidase in Patients With Guillain-Barré Syndrome
NCT04846010PHASE1/PHASE2UNKNOWNRecovering Damaged Cells for Sequelae Caused by COVID-19, SARS-CoV-2
NCT05701189PHASE2WITHDRAWNEvaluating Efgartigimod in Patients With Guillain-Barré Syndrome
NCT03773328PHASE1WITHDRAWNA Clinical Trial of CK0801 (a New Drug) In Patients With Treatment-Resistant Guillain-Barré Syndrome (GBS)
NCT04035135PHASE1COMPLETEDA Clinical Study of ANX005 and IVIG in Subjects With Guillain Barré Syndrome (GBS)
NCT06334796EARLY_PHASE1COMPLETEDArtificial Intelligence-powered Virtual Assistant for Emergency Triage in Neurology
NCT04829526Not specifiedRECRUITINGFirm Observational Clinical Unicenter Study on Guillain Barré Syndrome
NCT04871035Not specifiedRECRUITINGImmunoadsorption Versus Plasma Exchange for Treatment of Guillain-Barré Syndrome (GBS)
NCT05114941Not specifiedNOT_YET_RECRUITINGComparison of the Efficacy and Safety of Immunoadsorption and Intravenous Immunoglobulin for Guillain-Barre Syndrome
NCT05461898Not specifiedRECRUITINGRehabGBs: Rehabilitation in People With Guillain-Barré Syndrome
NCT06167239Not specifiedRECRUITINGVentilator Trigger Sensitivity Adjustment Versus Threshold Inspiratory Muscle Training on Arterial Blood Gases
NCT06502015Not specifiedRECRUITINGBiomarkers in Autoimmune Disease of Nervous System
NCT06605612Not specifiedENROLLING_BY_INVITATIONDevelopment and Validation of the FBIndex to Determine the Risk of Falls for Patients With Neuromuscular Disorders
NCT06612242Not specifiedRECRUITINGEarly vs. Late Tracheostomy in Patients With Guillain -Barre Syndrome
NCT06615622Not specifiedRECRUITINGOur Study Aims to Determine if Nerve Alterations in Acute GBS and CIDP Detectable by Ultrasound Match Electrodiagnostic Findings and if This Method Aids Early Diagnosis, Predict Their Outcomes and Differentiate Between Axonal and Demyelinating Subtypes.
NCT06740656Not specifiedNOT_YET_RECRUITINGNeuromuscular Complications of MEK Inhibitors: a French Case Series and a Systematic Review of the Literature
NCT06822231Not specifiedRECRUITINGHigh-Tech Rehabilitation Pathway for Acute Adult Neuromuscular Diseases - Fit4MedRob-Acute MND Project
NCT06940908Not specifiedRECRUITINGLiving With Guillain-Barré Syndrome as Children.
NCT06996509Not specifiedRECRUITINGNoninvasive Support for Acute Respiratory Failure in Guillain-Barré Syndrome
NCT07072676Not specifiedENROLLING_BY_INVITATIONThe Use of Assistive Gait Devices Can Reduce the Risk of Falls in Patients With Neuromuscular Diseases Following a Training Period.
NCT07121985Not specifiedNOT_YET_RECRUITINGMultispectral Optoacoustic Imaging for the Detection of Inflammation and Damage of Peripheral Nerves in Guillain-Barré Syndrome and Chronic Inflammatory Demyelinating Polyneuropathy
NCT00004833Not specifiedTERMINATEDRandomized Study of Plasmapheresis or Human Immunoglobulin Infusion in Childhood Guillain-Barre Syndrome
NCT00173199Not specifiedUNKNOWNThe Changes of Cytokines in Guillain Barré Syndrome: the Correlation With Clinical Manifestations and Skin Innervation
NCT00575653Not specifiedCOMPLETEDSafety Study of GBS Following Menactra Meningococcal Vaccination
NCT01005524Not specifiedCOMPLETEDBrain Computer Interface for Communication in ICU: a Feasibility Study
NCT01306578Not specifiedCOMPLETEDIntravenous Immunoglobulin (IVIG) Versus Plasma Exchange (PE) for Ventilated Children With Guillain Barre Syndrome (GBS)
NCT01370200Not specifiedCOMPLETEDRegional Citrate Anticoagulation in Plasma Exchange Treatment

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
EFGARTIGIMOD ALFA42
CROVALIMAB41
DALFAMPRIDINE41
ECULIZUMAB41
HUMAN IMMUNOGLOBULIN G41
IMLIFIDASE41
ANX-00532
FIBRINOGEN, HUMAN31