Lecanemab
drugOn this page
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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL3833321 |
| Name | Lecanemab |
| Type | Antibody |
| Max phase | 4 |
| ATC | N06DX04 |
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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| Alzheimer disease | 4 | MONDO:0004975 | MONDO:0004975 |
| dementia | 4 | MONDO:0001627 | HP:0000726 |
Clinical trials
Total trials: 19.
Phase distribution
| Phase | Trials |
|---|---|
| Not specified | 6 |
| PHASE3 | 3 |
| PHASE2 | 3 |
| PHASE1 | 3 |
| PHASE2/PHASE3 | 2 |
| PHASE4 | 1 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT07604896 | PHASE4 | RECRUITING | Evaluating the Efficacy and Safety of Lecanemab in Alzheimer’s Disease Through Multi-omics Approachs |
| NCT01760005 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | Dominantly 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 |
| NCT04468659 | PHASE3 | ACTIVE_NOT_RECRUITING | AHEAD 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 |
| NCT05269394 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | Dominantly 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) |
| NCT06384573 | PHASE3 | ACTIVE_NOT_RECRUITING | DIAN-TU Amyloid Removal Trial (ART) in Dominantly Inherited Alzheimer’s Disease |
| NCT06530732 | PHASE3 | RECRUITING | Deep Cervical Lymphatlc-Venous Anastomosis Surgery for the Treatment of Alzheimer’s Disease: A Pilot Study (DIVA Study) |
| NCT06602258 | PHASE2 | ACTIVE_NOT_RECRUITING | A Study of E2814 With Concurrent Lecanemab Treatment in Participants With Early Alzheimer’s Disease |
| NCT07212062 | PHASE2 | NOT_YET_RECRUITING | The 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. |
| NCT01767311 | PHASE2 | COMPLETED | A Study to Evaluate Safety, Tolerability, and Efficacy of Lecanemab in Subjects With Early Alzheimer’s Disease |
| NCT02094729 | PHASE1 | COMPLETED | A 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 |
| NCT05045716 | PHASE1 | COMPLETED | A Study of Subcutaneous Lecanemab in Healthy Participants |
| NCT05533801 | PHASE1 | COMPLETED | A Study to Demonstrate the Bioequivalence of Lecanemab Supplied in Vials and a Single-Use Auto-Injector (AI) in Healthy Participants |
| NCT05469009 | EARLY_PHASE1 | ACTIVE_NOT_RECRUITING | Safety 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 |
| NCT05925621 | Not specified | RECRUITING | Cognitive Neurology Unit Clinical Registry |
| NCT06285448 | Not specified | ENROLLING_BY_INVITATION | Feasibility of Lecanemab Registry and Clinical Outcome Measures |
| NCT06741553 | Not specified | RECRUITING | Prospective Cohort Study of Patients With Early Alzheimer’s Disease Treated With Lecanemab |
| NCT07152418 | Not specified | NOT_YET_RECRUITING | Therapeutic Efficacy of Monoclonal Antibody Drugs for Alzheimer’s Disease Based on PET Research |
| NCT07505095 | Not specified | NOT_YET_RECRUITING | Efficacy of Lecanemab at Different Therapeutic Doses for Alzheimer’s Disease (AD) in Real-World Practice |
| NCT07544953 | Not specified | NOT_YET_RECRUITING | Amyloid 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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: Alzheimer disease, dementia