Amivantamab
ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: amivantamab-vmjw, CNTO4424, JNJ 61186372, JNJ-6372, rybrevant
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Amivantamab is a drug catalogued in DrugCentral. It was first approved by the FDA in 2021. DrugCentral lists 2 molecular targets, including MET and EGFR. Recorded indications include Advanced or metastatic non-small cell lung cancer with EGFR exon 20 insertion mutations.
- Molecular targets: MET and EGFR (2 listed in DrugCentral).
- Indications: Advanced or metastatic non-small cell lung cancer with EGFR exon 20 insertion mutations.
- ATC code: L01FX18 (Other monoclonal antibodies and antibody drug conjugates).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Advanced or metastatic non-small cell lung cancer with EGFR exon 20 insertion mutations
Mechanism & targets
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Hepatocyte growth factor receptor | MET | other | Kd 10.40 |
| Epidermal growth factor receptor | EGFR | other | Kd 8.84 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2021-09-12 | EMA | — | Janssen-Cilag International N.V. | |
| 2021-05-21 | FDA | — | JANSSEN BIOTECH |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L01FX18 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES › Other monoclonal antibodies and antibody drug conjugates |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label: EGFR · Testing Required
- FDA label: EGFR · Testing Required
- HCSC label: EGFR · 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 |
|---|---|
| Infusion related reaction | 1622.3 |
| Paronychia | 665.0 |
| Rash | 510.1 |
| Dermatitis acneiform | 379.3 |
| Skin toxicity | 332.9 |
| Non-small cell lung cancer | 220.7 |
| Hypoalbuminaemia | 163.6 |
| Mucosal inflammation | 128.4 |
| Pulmonary embolism | 120.9 |
| Pneumonitis | 114.4 |
| Flushing | 99.4 |
| Embolism venous | 94.9 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | — |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Amivantamab used for?
DrugCentral lists the following indications for Amivantamab: Advanced or metastatic non-small cell lung cancer with EGFR exon 20 insertion mutations.
How does Amivantamab work?
Its molecular targets in DrugCentral include MET and EGFR.
When was Amivantamab first approved?
Amivantamab was first approved by the FDA in 2021.
Browse: all drugs starting with A · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5463 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL4297774 — compound record and bioactivity
- DrugBank DB16695 — drug record
- FDA UNII 0JSR7Z0NB6 — substance identity
- DailyMed: FDA labels for Amivantamab — current prescribing information (label search)
- UniProt P08581 (MET) — target protein
- UniProt P00533 (EGFR) — 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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