Envafolimab
Envafolimab is an antibody pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against programmed cell death 1 ligand 1.
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Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Indications
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Clinical
Clinical Trials
51 clinical trials
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Indications Phases 4
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Non-small-cell lung carcinoma | D002289 | 1 | 9 | — | — | — | 9 | ||
| Neoplasms | D009369 | C80 | 4 | 3 | — | — | 2 | 8 | |
| Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 1 | 2 | — | — | — | 2 |
| Hiv infections | D015658 | EFO_0000764 | B20 | — | 2 | — | — | — | 2 |
| Sarcoma | D012509 | 1 | 2 | — | — | — | 2 | ||
| Chronic hepatitis b | D019694 | EFO_0004197 | B18.1 | — | 1 | — | — | — | 1 |
| Multiple primary neoplasms | D009378 | — | 1 | — | — | — | 1 | ||
| Renal cell carcinoma | D002292 | 1 | 1 | — | — | — | 1 | ||
| Endometrial neoplasms | D016889 | EFO_0004230 | — | 1 | — | — | — | 1 | |
| Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | — | 1 | — | — | — | 1 |
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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 | ENVAFOLIMAB |
| INN | envafolimab |
| Description | Envafolimab is an antibody pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against programmed cell death 1 ligand 1. |
| Classification | Antibody |
| Drug class | monoclonal antibodies |
| Image (chem structure or protein) | |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL4298006 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | — |
| UNII ID | ES1M06M6QH (ChemIDplus, GSRS) |
Target
Agency Approved
CD274
CD274
Alternate
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Variants
Clinical Variant
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Financial
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Trends
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Additional graphs summarizing 101 documents
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Safety
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0 adverse events reported
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