Opdualag(relatlimab)
Opdualag (relatlimab) is an antibody pharmaceutical. Relatlimab was first approved as Opdualag on 2022-03-18. It is used to treat melanoma in the USA. It has been approved in Europe to treat melanoma. The pharmaceutical is active against lymphocyte activation gene 3 protein.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
neoplasms | D009369 |
Trade Name
FDA
EMA
Combinations
Opdualag
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)
Nivolumab
+
Relatlimab
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Opdualag | nivolumab and relatlimab-rmbw | Bristol-Myers Squibb Company | N-761234 RX | 2022-03-18 | 1 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
opdualag | Biologic Licensing Application | 2022-03-18 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
melanoma | — | D008545 | — |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
nivolumab / relatlimab, Opdualag, Bristol-Myers Squibb Company | |||
2029-03-18 | Orphan excl. |
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
57 clinical trials
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Indications Phases 4
No data
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Neoplasms | D009369 | C80 | 7 | 7 | — | — | — | 12 | |
Stomach neoplasms | D013274 | EFO_0003897 | C16 | 1 | 4 | — | — | — | 5 |
Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 3 | 3 | — | — | — | 5 |
Squamous cell carcinoma of head and neck | D000077195 | 1 | 2 | — | — | — | 3 | ||
Uveal neoplasms | D014604 | EFO_1001230 | 1 | 2 | — | — | — | 3 | |
Non-small-cell lung carcinoma | D002289 | 1 | 2 | — | — | — | 3 | ||
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | 1 | 2 | — | — | — | 2 |
Esophageal neoplasms | D004938 | C15 | 1 | 1 | — | — | — | 2 | |
Colonic neoplasms | D003110 | C18 | — | 2 | — | — | — | 2 | |
Non-hodgkin lymphoma | D008228 | C85.9 | 2 | 2 | — | — | — | 2 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Glioblastoma | D005909 | EFO_0000515 | 2 | — | — | — | — | 2 | |
Brain neoplasms | D001932 | EFO_0003833 | C71 | 1 | — | — | — | — | 1 |
Gliosarcoma | D018316 | 1 | — | — | — | — | 1 | ||
Castration-resistant prostatic neoplasms | D064129 | 1 | — | — | — | — | 1 | ||
Urologic neoplasms | D014571 | C64-C68 | 1 | — | — | — | — | 1 | |
Neoplasm metastasis | D009362 | EFO_0009708 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | RELATLIMAB |
INN | relatlimab |
Description | Relatlimab is a monoclonal antibody designed for the treatment of melanoma. It is used in combination with nivolumab to treat melanoma.
|
Classification | Antibody |
Drug class | monoclonal antibodies |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | — |
RxCUI | — |
ChEMBL ID | CHEMBL3990044 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB14851 |
UNII ID | AF75XOF6W3 (ChemIDplus, GSRS) |
Target
Variants
Clinical Variant
No data
Financial
Opdualag - Bristol Myers Squibb
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€
£
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 772 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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130 adverse events reported
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