Olumiant(baricitinib)
Olumiant (baricitinib) is a small molecule pharmaceutical. Baricitinib was first approved as Olumiant on 2017-02-13. It is used to treat rheumatoid arthritis in the USA. It has been approved in Europe to treat rheumatoid arthritis. The pharmaceutical is active against tyrosine-protein kinase JAK1 and tyrosine-protein kinase JAK2. In addition, it is known to target cyclin-G-associated kinase, non-receptor tyrosine-protein kinase TYK2, BMP-2-inducible protein kinase, AP2-associated protein kinase 1, and tyrosine-protein kinase JAK3.
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Commercial
Trade Name
FDA
EMA
Olumiant
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Baricitinib
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
OLUMIANT | Eli Lilly | N-207924 RX | 2018-05-31 | 3 products, RLD |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
olumiant | New Drug Application | 2020-11-19 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
rheumatoid arthritis | EFO_0000685 | D001172 | M06.9 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
BARICITINIB, OLUMIANT, ELI LILLY AND CO | |||
2025-06-13 | I-890 | ||
2025-05-10 | I-891 | ||
2023-05-31 | NCE |
HCPCS
No data
Clinical
Clinical Trials
124 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 | 1 | 4 | 9 | 5 | 4 | 23 |
Covid-19 | D000086382 | U07.1 | — | 6 | 11 | 1 | 4 | 19 | |
Psoriatic arthritis | D015535 | EFO_0003778 | L40.5 | — | — | — | 1 | — | 1 |
Spondylarthritis | D025241 | — | — | — | 1 | — | 1 | ||
Systemic scleroderma | D012595 | EFO_0000717 | M34 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Atopic dermatitis | D003876 | EFO_0000274 | L20 | — | 1 | 8 | — | 1 | 10 |
Systemic lupus erythematosus | D008180 | EFO_0002690 | M32 | — | 1 | 3 | — | — | 4 |
Pneumonia | D011014 | EFO_0003106 | J18 | — | 3 | 2 | — | — | 4 |
Dermatomyositis | D003882 | EFO_0000398 | M33 | — | 2 | 1 | — | 1 | 4 |
Juvenile arthritis | D001171 | EFO_0002609 | M08 | — | — | 3 | — | — | 3 |
Alopecia areata | D000506 | EFO_0004192 | L63 | — | 1 | 3 | — | — | 3 |
Skin diseases | D012871 | L00-L99 | — | 2 | 1 | — | — | 3 | |
Respiratory distress syndrome | D012128 | EFO_1000637 | J80 | — | 1 | 2 | — | — | 2 |
Lipodystrophy | D008060 | E88.1 | — | 1 | 1 | — | 1 | 2 | |
Uveitis | D014605 | EFO_1001231 | H20.9 | — | — | 1 | — | — | 1 |
Show 7 more
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Graft vs host disease | D006086 | D89.81 | 2 | 1 | — | — | — | 2 | |
Psoriasis | D011565 | EFO_0000676 | L40 | — | 1 | — | — | 1 | 2 |
Sjogren's syndrome | D012859 | EFO_0000699 | M35.0 | 1 | 2 | — | — | — | 2 |
Vitiligo | D014820 | EFO_0004208 | L80 | — | 1 | — | — | — | 1 |
Type 1 diabetes mellitus | D003922 | EFO_0001359 | E10 | — | 1 | — | — | — | 1 |
Sars-cov-2 | D000086402 | — | 1 | — | — | — | 1 | ||
Myositis | D009220 | EFO_0000783 | G72.49 | — | 1 | — | — | — | 1 |
Biliary liver cirrhosis | D008105 | K74.3 | — | 1 | — | — | — | 1 | |
Giant cell arteritis | D013700 | EFO_1001209 | M31.6 | — | 1 | — | — | — | 1 |
Diabetic nephropathies | D003928 | EFO_0000401 | — | 1 | — | — | — | 1 |
Show 12 more
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Respiratory insufficiency | D012131 | HP_0002093 | J96.9 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | BARICITINIB |
INN | baricitinib |
Description | Baricitinib is a pyrrolopyrimidine that is 7H-pyrrolo[2,3-d]pyrimidine substituted by a 1-[3-(cyanomethyl)-1-(ethanesulfonyl)azetidin-3-yl]-1H-pyrazol-4-yl group at position 5. It is an FDA approved selective Janus Kinase 1 and 2 (JAK1 and JAK2) inhibitor used for the treatment of rheumatoid arthritis. It has a role as an antirheumatic drug, an EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor, an anti-inflammatory agent, an immunosuppressive agent and an antiviral agent. It is a pyrrolopyrimidine, a member of pyrazoles, a member of azetidines, a sulfonamide and a nitrile. |
Classification | Small molecule |
Drug class | tyrosine kinase inhibitors: tyrosine kinase inhibitors; janus kinase inhibitors |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CCS(=O)(=O)N1CC(CC#N)(n2cc(-c3ncnc4[nH]ccc34)cn2)C1 |
Identifiers
PDB | 4W9X |
CAS-ID | 1187594-09-7 |
RxCUI | 2047232 |
ChEMBL ID | CHEMBL2105759 |
ChEBI ID | — |
PubChem CID | 44205240 |
DrugBank | DB11817 |
UNII ID | ISP4442I3Y (ChemIDplus, GSRS) |
Target
Variants
Clinical Variant
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Financial
Olumiant - Eli Lilly
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Olumiant - Incyte
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 7,001 documents
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Safety
Black-box Warning
Black-box warning for: Olumiant
Adverse Events
Top Adverse Reactions
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1,509 adverse events reported
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