Jakafi, Jakavi(ruxolitinib)
Jakafi, Jakavi, Opzelura (ruxolitinib) is a small molecule pharmaceutical. Ruxolitinib was first approved as Jakafi on 2011-11-16. It is used to treat polycythemia vera and primary myelofibrosis in the USA. It has been approved in Europe to treat graft vs host disease, myeloproliferative disorders, polycythemia vera, and vitiligo. The pharmaceutical is active against tyrosine-protein kinase JAK1 and tyrosine-protein kinase JAK2. In addition, it is known to target tyrosine-protein kinase JAK3 and non-receptor tyrosine-protein kinase TYK2.
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COVID-19
Novartis Pharmaceuticals
Top 200 Pharmaceuticals by Retail Sales
Commercial
Trade Name
FDA
EMA
Jakafi, Opzelura
Drug Products
FDA
EMA
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
RUXOLITINIB PHOSPHATE, JAKAFI, INCYTE CORP | |||
2029-03-22 | PED | ||
2028-09-22 | ODE-373 | ||
2026-11-24 | PED | ||
2026-06-19 | PED | ||
2026-05-24 | ODE-238 | ||
2025-12-19 | M-285 | ||
2025-03-22 | PED | ||
2024-09-22 | I-872 | ||
RUXOLITINIB PHOSPHATE, OPZELURA, INCYTE CORP | |||
2026-01-18 | PED | ||
2025-07-18 | I-896 | ||
2025-03-21 | PED | ||
2024-09-21 | NP |
Patent Expiration
Patent | Expires | Flag | FDA Information |
---|---|---|---|
Ruxolitinib Phosphate, Opzelura, Incyte Corp | |||
11602536 | 2041-05-05 | U-3550 | |
11510923 | 2040-09-04 | U-3505 | |
11590137 | 2040-09-04 | U-3505 | |
11590138 | 2040-06-10 | U-3551 | |
10758543 | 2031-05-20 | DP | |
10869870 | 2031-05-20 | U-3229, U-3404 | |
11219624 | 2031-05-20 | DP | U-3229 |
11571425 | 2031-05-20 | DP | |
11590136 | 2031-05-20 | U-3229, U-3404 | |
10610530 | 2028-06-12 | U-3229, U-3404 | |
9974790 | 2026-12-12 | U-3229, U-3404 | |
10639310 | 2026-12-12 | U-3229 | |
Ruxolitinib Phosphate, Jakafi, Incyte Corp | |||
8722693 | 2028-06-12 | DS, DP | |
8822481 | 2028-06-12 | U-1573, U-3226, U-3227, U-3228, U-3229, U-3230, U-3404 | |
8829013 | 2028-06-12 | U-1201, U-1622, U-3227, U-3228 | |
10016429 | 2028-06-12 | U-3226, U-3230 | |
7598257 | 2027-12-24 | DS, DP | U-3227, U-3228 |
8415362 | 2027-12-24 | DS, DP | |
9079912 | 2026-12-12 | U-3226, U-3227, U-3228, U-3229, U-3230, U-3404 | |
9814722 | 2026-12-12 | U-3226, U-3230 |
HCPCS
No data
Clinical
Clinical Trials
299 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Primary myelofibrosis | D055728 | D47.4 | 32 | 36 | 10 | 3 | 6 | 73 | |
Polycythemia vera | D011087 | D45 | 4 | 8 | 5 | 1 | 4 | 19 | |
Graft vs host disease | D006086 | D89.81 | 2 | 9 | 1 | 2 | 3 | 16 | |
Myeloid leukemia acute | D015470 | C92.0 | 7 | 9 | — | 1 | — | 14 | |
Atopic dermatitis | D003876 | EFO_0000274 | L20 | 3 | 3 | 4 | 1 | — | 11 |
Hemophagocytic lymphohistiocytosis | D051359 | D76.1 | 2 | 3 | 1 | 2 | — | 6 | |
Healthy volunteers/patients | — | 1 | — | — | 2 | — | 3 | ||
Beta-thalassemia | D017086 | Orphanet_848 | D56.1 | — | 1 | — | 1 | — | 2 |
Cytokine release syndrome | D000080424 | D89.83 | — | 1 | — | 1 | — | 2 | |
T-cell lymphoma | D016399 | 1 | — | — | 1 | — | 2 |
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Covid-19 | D000086382 | U07.1 | 2 | 10 | 4 | — | 3 | 16 | |
Precursor cell lymphoblastic leukemia-lymphoma | D054198 | C91.0 | 6 | 6 | 1 | — | — | 11 | |
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 3 | 2 | 2 | — | — | 7 |
Essential thrombocythemia | D013920 | D47.3 | 2 | 7 | 1 | — | — | 7 | |
Vitiligo | D014820 | EFO_0004208 | L80 | — | 4 | 1 | — | — | 5 |
Sars-cov-2 | D000086402 | 1 | 2 | 1 | — | 1 | 3 | ||
Severe acute respiratory syndrome-related coronavirus | D045473 | NCBITaxon_227859 | — | 1 | 1 | — | — | 1 | |
Macrophage activation syndrome | D055501 | EFO_1001806 | — | — | 1 | — | — | 1 | |
Eczema | D004485 | HP_0000964 | L30.9 | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Myelodysplastic syndromes | D009190 | D46 | 5 | 5 | — | — | — | 9 | |
Neoplasms | D009369 | C80 | 6 | 6 | — | — | — | 9 | |
Breast neoplasms | D001943 | EFO_0003869 | C50 | 4 | 6 | — | — | — | 8 |
Hodgkin disease | D006689 | C81 | 4 | 3 | — | — | — | 6 | |
Leukemia | D007938 | C95 | 4 | 4 | — | — | — | 6 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 3 | 4 | — | — | — | 5 | |
Bcr-abl positive chronic myelogenous leukemia | D015464 | EFO_0000340 | 4 | 2 | — | — | — | 5 | |
Myeloid leukemia chronic-phase | D015466 | 3 | 3 | — | — | — | 5 | ||
Myeloproliferative disorders | D009196 | D47.1 | 5 | 4 | — | — | — | 5 | |
Hematologic neoplasms | D019337 | 1 | 3 | — | — | — | 4 |
Show 57 more
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Castration-resistant prostatic neoplasms | D064129 | 1 | — | — | — | — | 1 | ||
Residual neoplasm | D018365 | 1 | — | — | — | — | 1 | ||
Endometrial neoplasms | D016889 | EFO_0004230 | 1 | — | — | — | — | 1 | |
Uveal neoplasms | D014604 | EFO_1001230 | 1 | — | — | — | — | 1 | |
Triple negative breast neoplasms | D064726 | 1 | — | — | — | — | 1 | ||
Bone neoplasms | D001859 | EFO_0003820 | D16 | 1 | — | — | — | — | 1 |
Malaria | D008288 | EFO_0001068 | B54 | 1 | — | — | — | — | 1 |
Glioblastoma | D005909 | EFO_0000515 | 1 | — | — | — | — | 1 | |
Glioma | D005910 | EFO_0000520 | 1 | — | — | — | — | 1 | |
Cachexia | D002100 | HP_0004326 | R64 | 1 | — | — | — | — | 1 |
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Bone marrow neoplasms | D019046 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | RUXOLITINIB |
INN | ruxolitinib |
Description | Ruxolitinib is a pyrazole substituted at position 1 by a 2-cyano-1-cyclopentylethyl group and at position 3 by a pyrrolo[2,3-d]pyrimidin-4-yl group. Used as the phosphate salt for the treatment of patients with intermediate or high-risk myelofibrosis, including primary myelofibrosis, post-polycythemia vera myelofibrosis and post-essential thrombocythemia myelofibrosis. It has a role as an antineoplastic agent and an EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor. It is a nitrile, a pyrrolopyrimidine and a member of pyrazoles. |
Classification | Small molecule |
Drug class | deuterated compounds; tyrosine kinase inhibitors |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | N#CC[C@H](C1CCCC1)n1cc(-c2ncnc3[nH]ccc23)cn1 |
Identifiers
PDB | 4U5J |
CAS-ID | 941678-49-5 |
RxCUI | 1193326 |
ChEMBL ID | CHEMBL1789941 |
ChEBI ID | 66919 |
PubChem CID | 25126798 |
DrugBank | DB08877 |
UNII ID | 82S8X8XX8H (ChemIDplus, GSRS) |
Target
Alternate
JAK3
JAK3
TYK2
TYK2
Variants
Clinical Variant
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Financial
Opzelura - Incyte
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Jakafi - Incyte
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Jakavi - Incyte
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Jakavi - Novartis
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Trends
PubMed Central
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Additional graphs summarizing 9,811 documents
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Safety
Black-box Warning
Black-box warning for: Opzelura
Adverse Events
Top Adverse Reactions
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6,496 adverse events reported
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