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Cosentyx(secukinumab)
Cosentyx (secukinumab) is an antibody pharmaceutical. Secukinumab was first approved as Cosentyx on 2015-01-14. It is used to treat ankylosing spondylitis and psoriatic arthritis in the USA. It has been approved in Europe to treat ankylosing spondylitis, psoriasis, and psoriatic arthritis. The pharmaceutical is active against interleukin-17A.
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Novartis Pharmaceuticals
Top 200 Pharmaceuticals by Retail Sales
Commercial
Therapeutic Areas
Therapeutic Area
MeSH
musculoskeletal diseasesD009140
skin and connective tissue diseasesD017437
Trade Name
FDA
EMA
Cosentyx
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)
Secukinumab
Tradename
Proper name
Company
Number
Date
Products
CosentyxsecukinumabNovartis Pharmaceuticals CorporationN-125504 RX2015-01-21
4 products
Labels
FDA
EMA
Brand Name
Status
Last Update
cosentyxBiologic Licensing Application2020-06-16
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
ankylosing spondylitisEFO_0003898D013167M45
psoriatic arthritisEFO_0003778D015535L40.5
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
L: Antineoplastic and immunomodulating agents
L04: Immunosuppressants
L04A: Immunosuppressants
L04AC: Interleukin inhibitors
L04AC10: Secukinumab
HCPCS
No data
Clinical
Clinical Trials
193 clinical trials
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Mock data
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
PsoriasisD011565EFO_0000676L405827161469
Psoriatic arthritisD015535EFO_0003778L40.514144427
Ankylosing spondylitisD013167EFO_0003898M45295117
Rheumatoid arthritisD001172EFO_0000685M06.913317
Healthy volunteers/patients4115
Metabolic syndromeD024821EFO_0000195E88.8122
SpondylarthritisD025241112
Lamellar ichthyosisD017490Q80112
InflammationD00724911
BiopsyD00170611
Show 1 more
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hidradenitis suppurativaD017497L73.21315
UveitisD014605EFO_1001231H20.944
Giant cell arteritisD013700EFO_1001209M31.6123
Lupus nephritisD008181EFO_000576122
Juvenile arthritisD001171EFO_0002609M0822
TendinopathyD052256EFO_1001434M77.9112
Graves ophthalmopathyD049970EFO_100146611
Non-alcoholic fatty liver diseaseD065626EFO_0003095K75.8111
ArthritisD001168EFO_0005856M05-M1411
SpondylarthropathiesD025242EFO_0000706M4711
Show 2 more
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Atopic dermatitisD003876EFO_0000274L20213
Pyoderma gangrenosumD017511EFO_0006835L88122
Multiple sclerosisD009103EFO_0003885G3522
Crohn diseaseD003424EFO_0000384K5022
Covid-19D000086382U07.111
RosaceaD012393L71111
Lichen planusD008010L4311
Discoid lupus erythematosusD008179L93.011
Necrobiosis lipoidicaD00933511
Alopecia areataD000506EFO_0004192L6311
Show 13 more
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Pityriasis rubra pilarisD010916L44.011
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameSECUKINUMAB
INNsecukinumab
Description
Secukinumab (human mab)
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID875356-43-7
RxCUI1599788
ChEMBL IDCHEMBL1743068
ChEBI ID
PubChem CID
DrugBankDB09029
UNII IDDLG4EML025 (ChemIDplus, GSRS)
Target
Agency Approved
IL17A
IL17A
Organism
Homo sapiens
Gene name
IL17A
Gene synonyms
CTLA8, IL17
NCBI Gene ID
Protein name
interleukin-17A
Protein synonyms
CTLA-8, Cytotoxic T-lymphocyte-associated antigen 8, cytotoxic T-lymphocyte-associated protein 8, interleukin 17 (cytotoxic T-lymphocyte-associated serine esterase 8), interleukin-17
Uniprot ID
Mouse ortholog
Il17a (16171)
interleukin-17A (Q62386)
Alternate
No data
Variants
Clinical Variant
No data
Financial
Cosentyx - Novartis
$
£
Mock data
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 5,527 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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7,531 adverse events reported
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