Lecanemab

drug
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Also known as Ban 2401BAN-2401BAN2401Lecanemab irmbLecanemab-irmbLeqembi

Summary

Lecanemab (CHEMBL3833321) is an approved antibody (ATC N06DX04); indicated across 2 conditions including alzheimer disease and dementia.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: N06DX04
  • Indications: 2 conditions
  • Clinical trials: 19

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3833321
NameLecanemab
TypeAntibody
Max phase4
ATCN06DX04

Also known as: Ban 2401, BAN-2401, BAN2401, Lecanemab, Lecanemab irmb, Lecanemab-irmb, Leqembi, LECANEMAB

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
Alzheimer disease4MONDO:0004975MONDO:0004975
dementia4MONDO:0001627HP:0000726

Clinical trials

Total trials: 19.

Phase distribution

PhaseTrials
Not specified6
PHASE33
PHASE23
PHASE13
PHASE2/PHASE32
PHASE41
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07604896PHASE4RECRUITINGEvaluating the Efficacy and Safety of Lecanemab in Alzheimer’s Disease Through Multi-omics Approachs
NCT01760005PHASE2/PHASE3ACTIVE_NOT_RECRUITINGDominantly Inherited Alzheimer Network Trial: An Opportunity to Prevent Dementia. A Study of Potential Disease Modifying Treatments in Individuals at Risk for or With a Type of Early Onset Alzheimer’s Disease Caused by a Genetic Mutation. Master Protocol DIAN-TU-001
NCT04468659PHASE3ACTIVE_NOT_RECRUITINGAHEAD 3-45 Study: A Study to Evaluate Efficacy and Safety of Treatment With Lecanemab in Participants With Preclinical Alzheimer’s Disease and Elevated Amyloid and Also in Participants With Early Preclinical Alzheimer’s Disease and Intermediate Amyloid
NCT05269394PHASE2/PHASE3ACTIVE_NOT_RECRUITINGDominantly Inherited Alzheimer Network Trial: An Opportunity to Prevent Dementia. A Study of Potential Disease Modifying Treatments in Individuals With a Type of Early Onset Alzheimer’s Disease Caused by a Genetic Mutation (DIAN-TU)
NCT06384573PHASE3ACTIVE_NOT_RECRUITINGDIAN-TU Amyloid Removal Trial (ART) in Dominantly Inherited Alzheimer’s Disease
NCT06530732PHASE3RECRUITINGDeep Cervical Lymphatlc-Venous Anastomosis Surgery for the Treatment of Alzheimer’s Disease: A Pilot Study (DIVA Study)
NCT06602258PHASE2ACTIVE_NOT_RECRUITINGA Study of E2814 With Concurrent Lecanemab Treatment in Participants With Early Alzheimer’s Disease
NCT07212062PHASE2NOT_YET_RECRUITINGThe Purpose of This Study is to Evaluate the Safety and Tolerability of X/T+X-EC in Participants With Alzheimer’s Disease Who Are Currently Treated With Lecanemab.
NCT01767311PHASE2COMPLETEDA Study to Evaluate Safety, Tolerability, and Efficacy of Lecanemab in Subjects With Early Alzheimer’s Disease
NCT02094729PHASE1COMPLETEDA Randomized, Double-blind, Placebo-controlled Study to Assess Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Pharmacodynamic Response of Repeated Intravenous Infusions of BAN2401 in Subjects With Mild Cognitive Impairment Due to Alzheimer’s Disease and Mild Alzheimer’s Disease
NCT05045716PHASE1COMPLETEDA Study of Subcutaneous Lecanemab in Healthy Participants
NCT05533801PHASE1COMPLETEDA Study to Demonstrate the Bioequivalence of Lecanemab Supplied in Vials and a Single-Use Auto-Injector (AI) in Healthy Participants
NCT05469009EARLY_PHASE1ACTIVE_NOT_RECRUITINGSafety and Feasibility of Exablate Blood-Brain Barrier Disruption for Mild Cognitive Impairment or Mild Alzheimer’s Disease Undergoing Standard of Care Monoclonal Antibody (mAb) Therapy
NCT05925621Not specifiedRECRUITINGCognitive Neurology Unit Clinical Registry
NCT06285448Not specifiedENROLLING_BY_INVITATIONFeasibility of Lecanemab Registry and Clinical Outcome Measures
NCT06741553Not specifiedRECRUITINGProspective Cohort Study of Patients With Early Alzheimer’s Disease Treated With Lecanemab
NCT07152418Not specifiedNOT_YET_RECRUITINGTherapeutic Efficacy of Monoclonal Antibody Drugs for Alzheimer’s Disease Based on PET Research
NCT07505095Not specifiedNOT_YET_RECRUITINGEfficacy of Lecanemab at Different Therapeutic Doses for Alzheimer’s Disease (AD) in Real-World Practice
NCT07544953Not specifiedNOT_YET_RECRUITINGAmyloid Monoclonal Antibody Treatment in PD Patients With Coexistent AD Pathology

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).