Monoclonal antibody | |
---|---|
Type | Whole antibody |
Source | Human |
Target | IL-12 and IL-23 |
Clinical data | |
Trade names | Stelara |
Other names | CNTO 1275 |
Biosimilars | ustekinumab-aekn,[1] ustekinumab-auub,[2] ustekinumab-srlf,[3] ustekinumab-ttwe,[4] Eksunbi,[5][6] Fymskina,[7][8] Imuldosa,[3] Jamteki,[9] Otulfi,[10][11][12] Pyzchiva,[4][13][14] Selarsdi,[1] Steqeyma,[15][16] Uzpruvo,[17] Wezlana,[2][18] Wezenla[19][20] |
AHFS/Drugs.com | Monograph |
MedlinePlus | a611013 |
License data |
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Pregnancy category | |
Routes of administration | Subcutaneous, intravenous |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Metabolism | unknown[24] |
Elimination half-life | 15–32 days (average 3 weeks)[24] |
Identifiers | |
CAS Number | |
DrugBank | |
ChemSpider |
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UNII | |
KEGG | |
ChEMBL | |
Chemical and physical data | |
Formula | C6482H10004N1712O2016S46 |
Molar mass | 145648.06 g·mol−1 |
(what is this?) (verify) |
Ustekinumab, sold under the brand name Stelara among others, is a monoclonal antibody medication developed by Janssen Pharmaceuticals, for the treatment of Crohn's disease, ulcerative colitis, plaque psoriasis and psoriatic arthritis,[27] targeting both IL-12 and IL-23.[28]
Ustekinumab is approved to treat Crohn's disease in the United States, Israel, Australia, and the European Union, and ulcerative colitis in the US, and in the EU to people who have not responded to more traditional treatments.[25][26][29][30] It was found not effective for multiple sclerosis.[31]
It is administered either by intravenous infusion or subcutaneous injection.[27] The antibody targets a subunit of human interleukin 12 and interleukin 23, which are naturally occurring proteins that regulate the immune system and immune-mediated inflammatory disorders.[32]
FDA Wezlana press release
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