Lecanemab
Amyloid Beta-directed Antibody — NERVOUS SYSTEM
Also known as: BAN2401, lecanemab-irmb, leqembi
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Lecanemab is a drug in the Amyloid Beta-directed Antibody class catalogued in DrugCentral. It was first approved by the FDA in 2023. Its mechanism of action is classified as Amyloid Beta-directed Antibody Interactions. DrugCentral lists 1 molecular target, including APP. Recorded indications include Alzheimer's disease.
- Drug class: Amyloid Beta-directed Antibody.
- Mechanism of action: Amyloid Beta-directed Antibody Interactions.
- Molecular targets: APP (1 listed in DrugCentral).
- Indications: Alzheimer's disease.
- ATC code: N06DX04 (Other anti-dementia drugs).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Alzheimer's disease
Mechanism & targets
| Mechanism of action (MoA) | Amyloid Beta-directed Antibody Interactions |
|---|---|
| Established pharmacologic class | Amyloid Beta-directed Antibody |
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Amyloid beta A4 protein | APP | other | IC50 6.22 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2023-01-06 | FDA | — | EISAI INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
N06DX04 | NERVOUS SYSTEM › PSYCHOANALEPTICS › ANTI-DEMENTIA DRUGS › Other anti-dementia drugs |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label
- FDA label: APOE · Testing Required
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Amyloid related imaging abnormality-oedema/effusion | 3245.3 |
| Amyloid related imaging abnormality-microhaemorrhages and haemosiderin deposits | 2937.8 |
| Amyloid related imaging abnormalities | 694.8 |
| Infusion related reaction | 499.6 |
| Superficial siderosis of central nervous system | 304.9 |
| Headache | 243.9 |
| Cerebral haemorrhage | 235.8 |
| Chills | 208.8 |
| Cerebral infarction | 187.6 |
| Cerebral microhaemorrhage | 123.2 |
| Confusional state | 91.4 |
| Subdural haematoma | 60.2 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 1260393-98-3 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Lecanemab used for?
DrugCentral lists the following indications for Lecanemab: Alzheimer's disease.
How does Lecanemab work?
Lecanemab is classified as Amyloid Beta-directed Antibody Interactions; its molecular targets in DrugCentral include APP.
When was Lecanemab first approved?
Lecanemab was first approved by the FDA in 2023.
What drug class does Lecanemab belong to?
Lecanemab is in the Amyloid Beta-directed Antibody class.
Browse: all drugs starting with L · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5717 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL3833321 — compound record and bioactivity
- DrugBank DB14580 — drug record
- FDA UNII 12PYH0FTU9 — substance identity
- DailyMed: FDA labels for Lecanemab — current prescribing information (label search)
- UniProt P05067 (APP) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
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