Canakinumab
ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: ACZ885, ilaris
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Canakinumab is a drug catalogued in DrugCentral. It was first approved by the FDA in 2009. DrugCentral lists 1 molecular target, including IL1B. Recorded indications include Articular gout, Cryopyrin associated periodic syndrome, Deficiency of mevalonate kinase and Familial Mediterranean fever.
- Molecular targets: IL1B (1 listed in DrugCentral).
- Indications: Articular gout, Cryopyrin associated periodic syndrome, Deficiency of mevalonate kinase, Familial Mediterranean fever and Systemic onset juvenile chronic arthritis and others.
- ATC code: L04AC08 (Interleukin inhibitors).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (6)
- Articular gout
- Cryopyrin associated periodic syndrome
- Deficiency of mevalonate kinase
- Familial Mediterranean fever
- Systemic onset juvenile chronic arthritis
- TNF receptor-associated periodic fever syndrome (TRAPS)
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2011-09-26 | PMDA | — | Novartis Pharma K.K. | Yes |
| 2009-10-23 | EMA | — | — | |
| 2009-06-17 | FDA | — | NOVARTIS PHARMS |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L04AC08 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSUPPRESSANTS › IMMUNOSUPPRESSANTS › Interleukin inhibitors |
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 |
|---|---|
| Apparent death | 1217.9 |
| Inappropriate schedule of product administration | 1156.5 |
| Haemophagocytic lymphohistiocytosis | 713.0 |
| Diverticulitis | 660.7 |
| Pyrexia | 429.3 |
| Pulmonary thrombosis | 409.0 |
| Deep vein thrombosis | 358.3 |
| Terminal state | 352.9 |
| Pulmonary embolism | 315.9 |
| Renal failure | 270.0 |
| Red blood cell sedimentation rate increased | 265.6 |
| Growth retardation | 259.0 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 914613-48-2 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Canakinumab used for?
DrugCentral lists the following indications for Canakinumab: Articular gout, Cryopyrin associated periodic syndrome, Deficiency of mevalonate kinase, Familial Mediterranean fever, Systemic onset juvenile chronic arthritis and TNF receptor-associated periodic fever syndrome (TRAPS).
How does Canakinumab work?
Its molecular targets in DrugCentral include IL1B.
When was Canakinumab first approved?
Canakinumab was first approved by the FDA in 2009.
Browse: all drugs starting with C · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 4952 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1201834 — compound record and bioactivity
- DrugBank DB06168 — drug record
- FDA UNII 37CQ2C7X93 — substance identity
- DailyMed: FDA labels for Canakinumab — current prescribing information (label search)
- UniProt P01584 (IL1B) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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