Adcetris(brentuximab vedotin)
Adcetris (brentuximab vedotin) is an antibody pharmaceutical. Brentuximab vedotin was first approved as Adcetris on 2011-08-19. It is used to treat hodgkin disease and large-cell lymphoma immunoblastic in the USA. It has been approved in Europe to treat hodgkin disease and non-hodgkin lymphoma. The pharmaceutical is active against tumor necrosis factor receptor superfamily member 8.
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Commercial
Trade Name
FDA
EMA
Adcetris
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)
Brentuximab vedotin
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Adcetris | brentuximab vedotin | Seagen Inc. | N-125388 RX | 2011-08-19 | 1 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
adcetris | Biologic Licensing Application | 2020-12-31 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
brentuximab vedotin, Adcetris, Seagen Inc. | |||
2029-11-10 | Orphan excl. |
Patent Expiration
No data
HCPCS
Code | Description |
---|---|
J9042 | Injection, brentuximab vedotin, 1 mg |
Clinical
Clinical Trials
170 clinical trials
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Indications Phases 3
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
T-cell lymphoma peripheral | D016411 | C84.9 | 5 | 8 | — | — | 2 | 14 | |
Lymphoma | D008223 | C85.9 | 3 | 6 | — | — | 1 | 8 | |
Sezary syndrome | D012751 | C84.1 | 2 | 2 | — | — | — | 4 | |
B-cell lymphoma | D016393 | 1 | 4 | — | — | — | 4 | ||
Enteropathy-associated t-cell lymphoma | D058527 | C86.2 | — | 4 | — | — | — | 4 | |
Adult t-cell leukemia-lymphoma | D015459 | C91.5 | 1 | 4 | — | — | — | 4 | |
Neoplasms | D009369 | C80 | 3 | 1 | — | — | — | 4 | |
Germ cell and embryonal neoplasms | D009373 | — | 3 | — | — | — | 3 | ||
Lymphomatoid papulosis | D017731 | C86.6 | — | 3 | — | — | — | 3 | |
Diffuse scleroderma | D045743 | EFO_0000404 | 1 | 3 | — | — | — | 3 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
T-cell leukemia | D015458 | 1 | — | — | — | — | 1 | ||
Recurrence | D012008 | 1 | — | — | — | — | 1 | ||
Myelodysplastic syndromes | D009190 | D46 | 1 | — | — | — | — | 1 | |
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | 1 | — | — | — | — | 1 |
Triple negative breast neoplasms | D064726 | 1 | — | — | — | — | 1 | ||
Stomach neoplasms | D013274 | EFO_0003897 | C16 | 1 | — | — | — | — | 1 |
Urinary bladder neoplasms | D001749 | C67 | 1 | — | — | — | — | 1 | |
Uterine cervical neoplasms | D002583 | 1 | — | — | — | — | 1 | ||
Hiv | D006678 | O98.7 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | BRENTUXIMAB VEDOTIN |
INN | brentuximab vedotin |
Description | Brentuximab Vedotin (chimeric mab) |
Classification | Antibody |
Drug class | synthetic analogs of the dolastatin series; monoclonal antibodies |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | 914088-09-8 |
RxCUI | 1147320 |
ChEMBL ID | CHEMBL1742994 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB08870 |
UNII ID | 7XL5ISS668 (ChemIDplus, GSRS) |
Target
Agency Approved
TNFRSF8
TNFRSF8
Organism
Homo sapiens
Gene name
TNFRSF8
Gene synonyms
CD30, D1S166E
NCBI Gene ID
Protein name
tumor necrosis factor receptor superfamily member 8
Protein synonyms
CD30, CD30L receptor, cytokine receptor CD30, Ki-1 antigen, Lymphocyte activation antigen CD30
Uniprot ID
Mouse ortholog
Tnfrsf8 (21941)
tumor necrosis factor receptor superfamily member 8 (Q60846)
Alternate
No data
Variants
Clinical Variant
No data
Financial
Adcetris - Seagen Inc.
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Adcetris - Takeda
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 4,452 documents
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Safety
Black-box Warning
Black-box warning for: Adcetris
Adverse Events
Top Adverse Reactions
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48 adverse events reported
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