Teplizumab
Tzield (teplizumab) is an antibody pharmaceutical. Teplizumab was first approved as Tzield on 2022-11-17. It is used to treat type 1 diabetes mellitus in the USA.
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Commercial
Therapeutic Areas
Trade Name
FDA
EMA
Tzield
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)
Teplizumab
Tradename | Proper name | Company | Number | Date | Products |
|---|---|---|---|---|---|
| Tzield | teplizumab-mzwv | Provention Bio | N-761183 RX | 2022-11-17 | 1 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| tzield | Biologic Licensing Application | 2025-05-06 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
|---|---|---|---|
| type 1 diabetes mellitus | EFO_0001359 | D003922 | E10 |
Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
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Clinical
Clinical Trials
38 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 |
|---|---|---|---|---|---|---|---|---|---|
| Diabetes mellitus | D003920 | EFO_0000400 | E08-E13 | — | — | 1 | — | — | 1 |
| Type 1 diabetes mellitus | D003922 | EFO_0001359 | E10 | — | — | 1 | — | — | 1 |
Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Teplizumab |
| INN | teplizumab |
| Description | Teplizumab (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 | CHEMBL1743078 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB06606 |
| UNII ID | S4M959U2IJ (ChemIDplus, GSRS) |
Target
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Financial
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Tzield – Sanofi
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Additional graphs summarizing 1,416 documents
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Safety
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348 adverse events reported
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