Ilaris(canakinumab)
Ilaris (canakinumab) is an antibody pharmaceutical. Canakinumab was first approved as Ilaris on 2009-06-17. It is used to treat cryopyrin-associated periodic syndromes, familial mediterranean fever, juvenile arthritis, and mevalonate kinase deficiency in the USA. It has been approved in Europe to treat cryopyrin-associated periodic syndromes, gouty arthritis, and juvenile arthritis. The pharmaceutical is active against interleukin-1 beta.
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Novartis Pharmaceuticals
Top 200 Pharmaceuticals by Retail Sales
Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
musculoskeletal diseases | D009140 |
nervous system diseases | D009422 |
hemic and lymphatic diseases | D006425 |
hereditary congenital and neonatal diseases and abnormalities | D009358 |
skin and connective tissue diseases | D017437 |
nutritional and metabolic diseases | D009750 |
immune system diseases | D007154 |
signs and symptoms pathological conditions | D013568 |
Trade Name
FDA
EMA
Ilaris
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Canakinumab
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Ilaris | canakinumab | Novartis Pharmaceuticals Corporation | N-125319 RX | 2016-12-22 | 1 products |
Show 1 discontinued
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
ilaris | Biologic Licensing Application | 2020-09-18 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
canakinumab, Ilaris, Novartis Pharmaceuticals Corporation | |||
2027-06-16 | Orphan excl. |
Patent Expiration
No data
HCPCS
Code | Description |
---|---|
J0638 | Injection, canakinumab, 1 mg |
Clinical
Clinical Trials
102 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Rheumatoid arthritis | D001172 | EFO_0000685 | M06.9 | 2 | 6 | — | 1 | — | 7 |
Psoriatic arthritis | D015535 | EFO_0003778 | L40.5 | — | — | — | 1 | — | 1 |
Spondylarthritis | D025241 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Juvenile arthritis | D001171 | EFO_0002609 | M08 | 1 | 1 | 7 | — | — | 8 |
Gouty arthritis | D015210 | — | 2 | 5 | — | — | 7 | ||
Cryopyrin-associated periodic syndromes | D056587 | M04.2 | — | — | 7 | — | — | 7 | |
Non-small-cell lung carcinoma | D002289 | 1 | 2 | 3 | — | — | 6 | ||
Type 2 diabetes mellitus | D003924 | EFO_0001360 | E11 | — | 4 | 2 | — | — | 5 |
Adult-onset still's disease | D016706 | EFO_0007135 | M06.1 | — | 1 | 1 | — | — | 2 |
Cytokine release syndrome | D000080424 | D89.83 | — | — | 1 | — | 1 | 2 | |
Atherosclerosis | D050197 | EFO_0003914 | I25.1 | — | 1 | 1 | — | — | 2 |
Lung neoplasms | D008175 | C34.90 | — | 1 | 1 | — | — | 2 | |
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | — | — | 1 | — | — | 1 |
Show 3 more
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Myelodysplastic syndromes | D009190 | D46 | 2 | 3 | — | — | — | 4 | |
Schnitzler syndrome | D019873 | EFO_1001165 | — | 3 | — | — | — | 3 | |
Covid-19 | D000086382 | U07.1 | — | 1 | — | — | 1 | 2 | |
Type 1 diabetes mellitus | D003922 | EFO_0001359 | E10 | — | 2 | — | — | — | 2 |
Melanoma | D008545 | — | 1 | — | — | — | 1 | ||
Familial mediterranean fever | D010505 | M04.1 | — | 1 | — | — | — | 1 | |
Gout | D006073 | EFO_0004274 | M10 | — | 1 | — | — | — | 1 |
Glucose intolerance | D018149 | HP_0000833 | R73.03 | — | 1 | — | — | — | 1 |
Knee osteoarthritis | D020370 | EFO_0004616 | M17 | — | 1 | — | — | — | 1 |
Alzheimer disease | D000544 | EFO_0000249 | F03 | — | 1 | — | — | — | 1 |
Show 29 more
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Triple negative breast neoplasms | D064726 | 2 | — | — | — | — | 2 | ||
Pancreatic ductal carcinoma | D021441 | 1 | — | — | — | — | 1 | ||
Renal cell carcinoma | D002292 | 1 | — | — | — | — | 1 | ||
Macular degeneration | D008268 | EFO_0001365 | H35.30 | 1 | — | — | — | — | 1 |
Healthy volunteers/patients | — | 1 | — | — | — | — | 1 | ||
Fever | D005334 | HP_0001945 | R50.9 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | CANAKINUMAB |
INN | canakinumab |
Description | Immunoglobulin G1, anti-[Homo sapiens interleukin 1, beta (IL1B)] human monoclonal ACZ885; gamma1 heavy chain (Homo sapiens VH-IGHG1*03) (221-214’)-disulfide with kappa light chain (Homo sapiens V-KAPPA-IGKC*01); (227-227’’:230-230’’)-bisdisulfide dimer |
Classification | Antibody |
Drug class | monoclonal antibodies |
Image (chem structure or protein) | ![]() |
Structure (InChI/SMILES or Protein Sequence) | >4G5Z:H|canakinumab antibody fragment heavy chain
QVQLVESGGGVVQPGRSLRLSCAASGFTFSVYGMNWVRQAPAKGLEWVAIIWYDGDNQYYADSVKGRFTISRDNSKNTLY
LQMNGLRAEDTAVYYCARDLRTGPFDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWN
SGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVAP
>4G5Z:L|canakinumab antibody fragment light chain
EIVLTQSPDFQSVTPKEKVTITCRASQSIGSSLHWYQQKPDQSPKLLIKYASQSFSGVPSRFSGSGSGTDFTLTINSLEA
EDAAAYYCHQSSSLPFTFGPGTKVDIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQ
ESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRG |
Identifiers
PDB | 4G5Z, 4G6J, 5BVJ, 5BVP |
CAS-ID | 914613-48-2 |
RxCUI | 853491 |
ChEMBL ID | CHEMBL1201834 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB06168 |
UNII ID | 37CQ2C7X93 (ChemIDplus, GSRS) |
Target
Alternate
No data
Variants
Clinical Variant
No data
Financial
Ilaris - Novartis
$
€
£
₣
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 7,397 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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2,849 adverse events reported
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