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
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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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
78 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Melanoma | D008545 | — | — | 4 | 9 | 4 | — | 1 | 17 |
| Colorectal neoplasms | D015179 | — | — | 1 | 3 | 1 | — | — | 5 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Neoplasms | D009369 | — | C80 | 7 | 8 | — | — | — | 13 |
| Stomach neoplasms | D013274 | EFO_0003897 | C16 | 1 | 5 | — | — | — | 6 |
| 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 |
| Hepatocellular carcinoma | D006528 | — | C22.0 | 2 | 1 | — | — | — | 3 |
| Non-small-cell lung carcinoma | D002289 | — | — | 1 | 2 | — | — | — | 3 |
| Urologic neoplasms | D014571 | — | C64-C68 | 1 | 2 | — | — | — | 3 |
| Ovarian neoplasms | D010051 | EFO_0003893 | C56 | 1 | 2 | — | — | — | 2 |
| Esophageal neoplasms | D004938 | — | C15 | 1 | 1 | — | — | — | 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 |
| 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
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Opdualag – Bristol Myers Squibb
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Estimated US medical usage
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Trends
PubMed Central
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Additional graphs summarizing 1,230 documents
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Safety
Black-box Warning
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Adverse Events
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162 adverse events reported
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