Pharmaceutical Information |
Drug Name |
Tocilizumab |
Drug ID |
BADD_D02234 |
Description |
Tocilizumab is a recombinant humanized monoclonal antibody IL-6 receptor inhibitor used to treat inflammatory and autoimmune conditions.[L12789] It was first described in the literature in 2003 when Chugai, a subsidiary of Roche began developing IL-6 inhibiting monoclonal antibodies.[A193281] It is currently being investigated to treat severely ill patients with COVID-19.[A193278,L12837,L12843]
Tocilizumab was granted FDA approval on 8 January 2010.[L12789] |
Indications and Usage |
Tocilizumab is indicated to treat moderate to severe rheumatoid arthritis, giant cell arteritis, polyarticular juvenile idiopathic arthritis, systemic juvenile idiopathic arthritis, and cytokine release syndrome.[L12789] |
Marketing Status |
approved |
ATC Code |
L04AC07 |
DrugBank ID |
DB06273
|
KEGG ID |
D02596
|
MeSH ID |
C502936
|
PubChem ID |
Not Available
|
TTD Drug ID |
D08HPZ
|
NDC Product Code |
50242-139; 50242-157; 50242-158; 50242-138; 50242-137; 50242-141; 71124-0019; 50242-136; 82143-004; 50242-143; 50242-135 |
UNII |
I031V2H011
|
Synonyms |
tocilizumab | atlizumab | monoclonal antibody, MRA | BAT-1806 | BAT1806 | MSB11456 | MSB-11456 | RG-1569 | R-1569 | RO-4877533 | Actemra | Roactemra | RHPM-1 |
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Chemical Information |
Molecular Formula |
Not Available |
CAS Registry Number |
375823-41-9 |
SMILES |
Not Available |
Chemical Structure |
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ADRs Induced by Drug |
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