Mogamulizumab
Poteligeo (mogamulizumab) is an antibody pharmaceutical. Mogamulizumab was first approved as Poteligeo on 2018-08-08. It is used to treat mycosis fungoides and sezary syndrome in the USA. It has been approved in Europe to treat mycosis fungoides and sezary syndrome. The pharmaceutical is active against C-C chemokine receptor type 4.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
|---|---|
| neoplasms | D009369 |
| hemic and lymphatic diseases | D006425 |
| immune system diseases | D007154 |
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| poteligeo | Biologic Licensing Application | 2025-03-13 |
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
Expiration | Code | ||
|---|---|---|---|
mogamulizumab, Poteligeo, Kyowa Kirin, Inc. | |||
| 2025-08-08 | Orphan excl. | ||
Patent Expiration
No data
HCPCS
Code | Description |
|---|---|
| J9204 | Injection, mogamulizumab-kpkc, 1 mg |
Clinical
Clinical Trials
39 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 |
|---|---|---|---|---|---|---|---|---|---|
| Lymphoma | D008223 | — | C85.9 | 3 | 9 | 1 | — | 1 | 13 |
| T-cell lymphoma peripheral | D016411 | — | — | 3 | 6 | 1 | — | — | 9 |
| T-cell lymphoma | D016399 | — | — | 3 | 5 | 1 | — | — | 8 |
| T-cell lymphoma cutaneous | D016410 | — | C84.A | 1 | 2 | 1 | — | 1 | 5 |
| Bone marrow diseases | D001855 | — | — | — | — | 1 | — | — | 1 |
| Spinal cord diseases | D013118 | — | G95.9 | — | — | 1 | — | — | 1 |
| Tropical spastic paraparesis | D015493 | EFO_0007527 | G04.1 | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Neoplasms | D009369 | — | C80 | 5 | 1 | — | — | — | 5 |
| Adult t-cell leukemia-lymphoma | D015459 | — | C91.5 | 1 | 3 | — | — | 1 | 5 |
| T-cell leukemia | D015458 | — | — | 1 | 3 | — | — | — | 4 |
| Leukemia | D007938 | — | C95 | — | 3 | — | — | — | 3 |
| Carcinoma | D002277 | — | C80.0 | 2 | 1 | — | — | — | 2 |
| Hepatocellular carcinoma | D006528 | — | C22.0 | 1 | 1 | — | — | — | 1 |
| Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 1 | 1 | — | — | — | 1 |
| Extranodal nk-t-cell lymphoma | D054391 | — | C86.0 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Lung neoplasms | D008175 | — | C34.90 | 2 | — | — | — | — | 2 |
| Mycoses | D009181 | — | B35-B49 | 1 | — | — | — | 1 | 2 |
| Mycosis fungoides | D009182 | — | C84.0 | 1 | — | — | — | 1 | 2 |
| Non-small-cell lung carcinoma | D002289 | — | — | 1 | — | — | — | — | 1 |
| Stomach neoplasms | D013274 | EFO_0003897 | C16 | 1 | — | — | — | — | 1 |
| Esophageal neoplasms | D004938 | — | C15 | 1 | — | — | — | — | 1 |
| Kidney neoplasms | D007680 | EFO_0003865 | C64 | 1 | — | — | — | — | 1 |
| Mouth neoplasms | D009062 | EFO_0003868 | C06.9 | 1 | — | — | — | — | 1 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Glioblastoma | D005909 | EFO_0000515 | — | — | — | — | — | 1 | 1 |
| Sezary syndrome | D012751 | — | C84.1 | — | — | — | — | 1 | 1 |
| Syndrome | D013577 | — | — | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Mogamulizumab |
| INN | mogamulizumab |
| Description | Mogamulizumab (humanized mab) |
| Classification | Antibody |
| Drug class | monoclonal antibodies |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL1743041 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB12498 |
| UNII ID | YI437801BE (ChemIDplus, GSRS) |
Target
Agency Approved
CCR4
CCR4
Alternate
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Variants
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Financial
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Trends
PubMed Central
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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1,506 adverse events reported
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