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 |
| skin and connective tissue diseases | D017437 |
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 | N-761234 RX | 2022-03-18 | 1 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| opdualag | Biologic Licensing Application | 2024-03-01 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
|---|---|---|---|
| non-small-cell lung carcinoma | — | D002289 | — |
| lymphoma | — | D008223 | C85.9 |
| urinary bladder neoplasms | — | D001749 | C67 |
| melanoma | — | D008545 | — |
| kidney neoplasms | EFO_0003865 | D007680 | C64 |
| squamous cell carcinoma | — | D002294 | — |
Agency Specific
FDA
EMA
Expiration | Code | ||
|---|---|---|---|
nivolumab / relatlimab, Opdualag, Bristol-Myers Squibb Company | |||
| 2029-03-18 | Orphan excl. | ||
Patent Expiration
No data
HCPCS
Code | Description |
|---|---|
| J9298 | Injection, nivolumab and relatlimab-rmbw, 3 mg/1 mg |
Clinical
Clinical Trials
94 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Melanoma | D008545 | — | — | 2 | 7 | 3 | — | — | 11 |
| Colorectal neoplasms | D015179 | — | — | — | 2 | 1 | — | — | 3 |
| Non-small-cell lung carcinoma | D002289 | — | — | — | 2 | 1 | — | — | 3 |
| Lung neoplasms | D008175 | — | C34.90 | — | 1 | 1 | — | — | 2 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Neoplasms | D009369 | — | C80 | 9 | 11 | — | — | — | 15 |
| Carcinoma | D002277 | — | C80.0 | 2 | 8 | — | — | — | 9 |
| Stomach neoplasms | D013274 | EFO_0003897 | C16 | 1 | 3 | — | — | — | 4 |
| Squamous cell carcinoma | D002294 | — | — | — | 3 | — | — | — | 3 |
| Renal cell carcinoma | D002292 | EFO_0000376 | — | — | 3 | — | — | — | 3 |
| Hepatocellular carcinoma | D006528 | — | C22.0 | 2 | 2 | — | — | — | 3 |
| Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 2 | 2 | — | — | — | 3 |
| Squamous cell carcinoma of head and neck | D000077195 | — | — | — | 2 | — | — | — | 2 |
| Recurrence | D012008 | — | — | 1 | 1 | — | — | — | 2 |
| Adenocarcinoma | D000230 | — | — | — | 2 | — | — | — | 2 |
Show 27 more
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Brain neoplasms | D001932 | EFO_0003833 | C71 | 2 | — | — | — | — | 2 |
| Esophageal neoplasms | D004938 | — | C15 | 1 | — | — | — | — | 1 |
| Glioblastoma | D005909 | EFO_0000515 | — | 1 | — | — | — | — | 1 |
| Gliosarcoma | D018316 | — | — | 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
No data
Financial
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Opdualag – Bristol Myers Squibb
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Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 1,793 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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653 adverse events reported
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