Oprelvekin
Neumega (oprelvekin) is a protein pharmaceutical. Oprelvekin was first approved as Neumega on 1997-11-25. The pharmaceutical is active against interleukin-6 receptor subunit beta.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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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)
Oprelvekin
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Neumega | oprelvekin | Wyeth | N-103694 DISCN | 1997-11-25 | 1 products |
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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HCPCS
Code | Description |
---|---|
J2355 | Injection, oprelvekin, 5 mg |
Clinical
Clinical Trials
18 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Pancytopenia | D010198 | HP_0001876 | D61.81 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Thrombocytopenia | D013921 | HP_0001873 | D69.6 | — | 3 | 1 | — | — | 3 |
Hematologic diseases | D006402 | EFO_0005803 | D75.9 | — | 1 | 1 | — | — | 1 |
Nasopharyngeal neoplasms | D009303 | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Von willebrand diseases | D014842 | D68.0 | — | 4 | — | — | — | 4 | |
Inflammatory bowel diseases | D015212 | EFO_0003767 | 1 | 1 | — | — | — | 2 | |
Leukemia | D007938 | C95 | — | 1 | — | — | — | 1 | |
Bcr-abl positive chronic myelogenous leukemia | D015464 | EFO_0000340 | — | 1 | — | — | — | 1 | |
Colorectal neoplasms | D015179 | — | 1 | — | — | — | 1 | ||
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 1 | 1 | — | — | — | 1 | |
B-cell lymphoma marginal zone | D018442 | C88.4 | 1 | 1 | — | — | — | 1 | |
Follicular lymphoma | D008224 | C82 | 1 | 1 | — | — | — | 1 | |
Waldenstrom macroglobulinemia | D008258 | C88.0 | 1 | 1 | — | — | — | 1 | |
Breast neoplasms | D001943 | EFO_0003869 | C50 | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Ulcerative colitis | D003093 | EFO_0000729 | K51 | 1 | — | — | — | — | 1 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Hemostatic disorders | D020141 | — | — | — | — | 1 | 1 | ||
Thrombocytopenic purpura idiopathic | D016553 | EFO_0007160 | D69.3 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | OPRELVEKIN |
INN | oprelvekin |
Description | Interleukin-11 precursor (IL-11) (Adipogenesis inhibitory factor) |
Classification | Protein |
Drug class | interleukins: interleukin-11 analogues and derivatives |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | 145941-26-0 |
RxCUI | 139994 |
ChEMBL ID | CHEMBL1201573 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB00038 |
UNII ID | HM5641GA6F (ChemIDplus, GSRS) |
Target
Agency Approved
IL6ST
IL6ST
Organism
Homo sapiens
Gene name
IL6ST
Gene synonyms
NCBI Gene ID
Protein name
interleukin-6 receptor subunit beta
Protein synonyms
CD130, CD130 antigen, CDw130, gp130, gp130 of the rheumatoid arthritis antigenic peptide-bearing soluble form, gp130, oncostatin M receptor, IL-6 receptor subunit beta, IL-6R subunit beta, interleukin receptor beta chain, Interleukin-6 signal transducer, Membrane glycoprotein 130, membrane glycoprotein gp130, Oncostatin-M receptor subunit alpha
Uniprot ID
Mouse ortholog
Il6st (16195)
interleukin-6 receptor subunit beta (Q00560)
Alternate
No data
Variants
Clinical Variant
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 143 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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92 adverse events reported
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